Works by Jabs, Ethylin Wang

Results: 61

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 505, doi. 10.1002/gepi.20323

By:

Sull, Jae Woong;
Liang, Kung-Yee;
Hetmanski, Jacqueline B.;
Fallin, Margaret Daniele;
Ingersoll, Roxann G.;
Park, Jiwan;
Wu-Chou, Yah-Huei;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Park, Beyoung Yun;
Jee, Sun Ha;
Jabs, Ethylin Wang;
Redett, Richard;
Jung, Euiju;
Ruczinski, Ingo;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

A Novel ZRS Mutation Leads to Preaxial Polydactyly Type 2 in a Heterozygous Form and Werner Mesomelic Syndrome in a Homozygous Form.

Published in:

Human Mutation, 2014, v. 35, n. 8, p. 945, doi. 10.1002/humu.22581

By:

VanderMeer, Julia E.;
Lozano, Reymundo;
Sun, Miao;
Xue, Yuan;
Daentl, Donna;
Jabs, Ethylin Wang;
Wilcox, William R.;
Ahituv, Nadav

Publication type:

Article

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.

Published in:

2009

By:

Paznekas, William A.;
Karczeski, Barbara;
Vermeer, Sascha;
Lowry, R. Brian;
Delatycki, Martin;
Laurence, Faivre;
Koivisto, Pasi A.;
Van Maldergem, Lionel;
Boyadjiev, Simeon A.;
Bodurtha, Joann N.;
Wang Jabs, Ethylin

Publication type:

Other

Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 6, p. 726, doi. 10.1038/ejhg.2009.228

By:

Ingersoll, Roxann G.;
Hetmanski, Jacqueline;
Ji-Wan Park;
Fallin, M. Daniele;
McIntosh, Iain;
Yah-Huei Wu-Chou;
Chen, Philip K.;
Yeow, Vincent;
Chong, Samuel S.;
Cheah, Felicia;
Jae Woong Sull;
Sun Ha Jee;
Hong Wang;
Tao Wu;
Murray, Tanda;
Shangzhi Huang;
Xiaoqian Ye;
Jabs, Ethylin Wang;
Redett, Richard;
Raymond, Gerald

Publication type:

Article

Parental origin of mutations in sporadic cases of Treacher Collins syndrome.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 9, p. 718, doi. 10.1038/sj.ejhg.5201029

By:

Splendore, Alessandra;
Jabs, Ethylin Wang;
Têmis Maria Félix;
Passos-Bueno, Maria Rita

Publication type:

Article

C-type natriuretic peptide analog treatment of craniosynostosis in a Crouzon syndrome mouse model.

Published in:

PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0201492

By:

Holmes, Greg;
Zhang, Lening;
Rivera, Joshua;
Murphy, Ryan;
Assouline, Claudia;
Sullivan, Lorraine;
Oppeneer, Todd;
Jabs, Ethylin Wang

Publication type:

Article

Roberts/pseudothalidomide syndrome and normal intelligence: approaches to diagnosis and management.

Published in:

1992

By:

Holden, Kenton R.;
Jabs, Ethylin Wang;
Sponseller, Paul D.;
Holden, K R;
Jabs, E W;
Sponseller, P D

Publication type:

journal article

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.

Published in:

Nature Genetics, 2012, v. 44, n. 12, p. 1360, doi. 10.1038/ng.2463

By:

Justice, Cristina M;
Yagnik, Garima;
Kim, Yoonhee;
Peter, Inga;
Jabs, Ethylin Wang;
Erazo, Monica;
Ye, Xiaoqian;
Ainehsazan, Edmond;
Shi, Lisong;
Cunningham, Michael L;
Kimonis, Virginia;
Roscioli, Tony;
Wall, Steven A;
Wilkie, Andrew O M;
Stoler, Joan;
Richtsmeier, Joan T;
Heuzé, Yann;
Sanchez-Lara, Pedro A;
Buckley, Michael F;
Druschel, Charlotte M

Publication type:

Article

Exome sequencing identifies the cause of a mendelian disorder.

Published in:

Nature Genetics, 2010, v. 42, n. 1, p. 30, doi. 10.1038/ng.499

By:

Ng, Sarah B.;
Buckingham, Kati J.;
Lee, Choli;
Bigham, Abigail W.;
Tabor, Holly K.;
Dent, Karin M.;
Huff, Chad D.;
Shannon, Paul T.;
Jabs, Ethylin Wang;
Nickerson, Deborah A.;
Shendure, Jay;
Bamshad, Michael J

Publication type:

Article

Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 468, doi. 10.1038/ng1548

By:

Vega, Hugo;
Waisfisz, Quinten;
Gordillo, Miriam;
Sakai, Norio;
Yanagihara, Itaru;
Yamada, Minoru;
Gosliga, Djoke van;
Kayserili, Hülya;
Xu, Chengzhe;
Ozono, Keiichi;
Jabs, Ethylin Wang;
Inui, Koji;
Joenje, Hans

Publication type:

Article

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome.

Published in:

Nature Genetics, 2004, v. 36, n. 3, p. 228, doi. 10.1038/ng1300

By:

Pandey, Amit V.;
Arlt, Wiebke;
Okuhara, Kouji;
Verge, Charles F.;
Jabs, Ethylin Wang;
Mendon&ccedila, Berenice B.;
Fujieda, Kenji;
Miller, Walter L.;
Flück, Christa E.;
Tajima, Toshihro

Publication type:

Article

Maternal periconceptional alcohol consumption and gastroschisis in the National Birth Defects Prevention Study, 1997–2011.

Published in:

Paediatric & Perinatal Epidemiology, 2022, v. 36, n. 6, p. 782, doi. 10.1111/ppe.12882

By:

Fisher, Sarah C.;
Howley, Meredith M.;
Romitti, Paul A.;
Desrosiers, Tania A.;
Jabs, Ethylin Wang;
Browne, Marilyn L.

Publication type:

Article

Single-cell analysis identifies a key role for Hhip in murine coronal suture development.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27402-5

By:

Holmes, Greg;
Gonzalez-Reiche, Ana S.;
Saturne, Madrikha;
Motch Perrine, Susan M.;
Zhou, Xianxiao;
Borges, Ana C.;
Shewale, Bhavana;
Richtsmeier, Joan T.;
Zhang, Bin;
van Bakel, Harm;
Jabs, Ethylin Wang

Publication type:

Article

Joint Testing of Genotypic and Gene-Environment Interaction Identified Novel Association for BMP4 with Non-Syndromic CL/P in an Asian Population Using Data from an International Cleft Consortium.

Published in:

PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109038

By:

Chen, Qianqian;
Wang, Hong;
Schwender, Holger;
Zhang, Tianxiao;
Hetmanski, Jacqueline B.;
Chou, Yah-Huei Wu;
Ye, Xiaoqian;
Yeow, Vincent;
Chong, Samuel S.;
Zhang, Bo;
Jabs, Ethylin Wang;
Parker, Margaret M.;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

Receptor Tyrosine Kinases Activate Canonical WNT/β-Catenin Signaling via MAP Kinase/LRP6 Pathway and Direct β-Catenin Phosphorylation.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035826

By:

Krejci, Pavel;
Aklian, Anie;
Kaucka, Marketa;
Sevcikova, Eva;
Prochazkova, Jirina;
Masek, Jan Kukla;
Mikolka, Pavol;
Pospisilova, Tereza;
Spoustova, Tereza;
Weis, MaryAnn;
Paznekas, William A.;
Wolf, Joshua H.;
Gutkind, J. Silvio;
Wilcox, William R.;
Kozubik, Alois;
Jabs, Ethylin Wang;
Bryja, Vitezslav;
Salazar, Lisa;
Vesela, Iva;
Balek, Lukas

Publication type:

Article

BMP4 Was Associated with NSCL/P in an Asian Population.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035347

By:

Chen, Qianqian;
Wang, Hong;
Hetmanski, Jacqueline B.;
Zhang, Tianxiao;
Ruczinski, Ingo;
Schwender, Holger;
Liang, Kung Yee;
Fallin, M. Daniele;
Redett, Richard J.;
Raymond, Gerald V.;
Chou, Yah- Huei Wu;
Chen, Philip Kuo-Ting;
Yeow, Vincent;
Chong, Samuel S.;
Cheah, Felicia S. H.;
Jabs, Ethylin Wang;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models.

Published in:

PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026425

By:

Martínez-Abadías, Neus;
Heuzé, Yann;
Yingli Wang;
Jabs, Ethylin Wang;
Aldridge, Kristina;
Richtsmeier, Joan T.

Publication type:

Article

Prenatal identification of small mosaic markers of different chromosomal origins.

Published in:

Prenatal Diagnosis, 1992, v. 12, n. 2, p. 83, doi. 10.1002/pd.1970120203

By:

Stetten, Gail;
Blakemore, Karin J.;
Courter, Anne M.;
Coss, Cathleen A.;
Jabs, Ethylin Wang

Publication type:

Article

Quantitative Assessment of Facial Asymmetry Using Three-Dimensional Surface Imaging in Adults: Validating the Precision and Repeatability of a Global Approach.

Published in:

Cleft Palate Craniofacial Journal, 2016, v. 53, n. 1, p. 126, doi. 10.1597/13-353

By:

Kornreich, Davida;
Mitchell, Adele A.;
Webb, Bryn D.;
Cristian, Ingrid;
Wang Jabs, Ethylin

Publication type:

Article

Mutational Screening of FGFR1, CER1, and CDON in a Large Cohort of Trigonocephalic Patients.

Published in:

Cleft Palate Craniofacial Journal, 2006, v. 43, n. 2, p. 148, doi. 10.1597/04-206.1

By:

Jehee, Fernanda Sarquis;
Alonso, Luis G.;
Cavalcanti, Denise P.;
Chong Kim;
Wall, Steven A.;
Mulliken, John B.;
Miao Sun;
Ethylin Wang Jabs;
Boyadjiev, Simeon A.;
Wilkie, Andrew O.M.;
Passos-Bueno, Maria Rita

Publication type:

Article

Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 11, p. 2743, doi. 10.1002/ajmg.a.63389

By:

Gates, Ryan W.;
Webb, Bryn D.;
Stevenson, David A.;
Jabs, Ethylin Wang;
DeFilippo, Colette;
Ruzhnikov, Maura R. Z.;
Tise, Christina G.

Publication type:

Article

Postnatal brain and skull growth in an Apert syndrome mouse model.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 745, doi. 10.1002/ajmg.a.35805

By:

Hill, Cheryl A.;
Martínez‐Abadías, Neus;
Motch, Susan M.;
Austin, Jordan R.;
Wang, Yingli;
Jabs, Ethylin Wang;
Richtsmeier, Joan T.;
Aldridge, Kristina

Publication type:

Article

Attitudes toward prenatal genetic testing for Treacher Collins syndrome among affected individuals and families.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1556, doi. 10.1002/ajmg.a.35379

By:

Wu, Rebecca L.;
Lawson, Cathleen S.;
Jabs, Ethylin Wang;
Sanderson, Saskia C.

Publication type:

Article

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 784, doi. 10.1002/ajmg.a.35257

By:

Shi, Min;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Ruczinski, Ingo;
Hetmanski, Jacqueline B.;
Wu, Tao;
Murray, Tanda;
Redett, Richard J.;
Wilcox, Allen J.;
Lie, Rolv T.;
Jabs, Ethylin Wang;
Wu-Chou, Yah Huei;
Chen, Philip K.;
Wang, Hong;
Ye, Xiaoqian;
Yeow, Vincent;
Chong, Samuel S.;
Shi, Bing;
Christensen, Kaare

Publication type:

Article

Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes.

Published in:

Brain: A Journal of Neurology, 2014, v. 137, n. 4, p. 1068, doi. 10.1093/brain/awu021

By:

Rucker, Janet C.;
Webb, Bryn D.;
Frempong, Tamiesha;
Gaspar, Harald;
Naidich, Thomas P.;
Jabs, Ethylin Wang

Publication type:

Article

A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3.

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 2, p. 522, doi. 10.1093/brain/aws345

By:

Chew, Sheena;
Balasubramanian, Ravikumar;
Chan, Wai-Man;
Kang, Peter B.;
Andrews, Caroline;
Webb, Bryn D.;
MacKinnon, Sarah E.;
Oystreck, Darren T.;
Rankin, Jessica;
Crawford, Thomas O.;
Geraghty, Michael;
Pomeroy, Scott L.;
Crowley, William F.;
Jabs, Ethylin Wang;
Hunter, David G.;
Grant, Patricia E.;
Engle, Elizabeth C.

Publication type:

Article

Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms.

Published in:

Human Genetics, 2009, v. 126, n. 3, p. 385, doi. 10.1007/s00439-009-0680-3

By:

Jae Woong Sull;
Kung-Yee Liang;
Hetmanski, Jacqueline B.;
Tao Wu;
Fallin, Margaret Daniele;
Ingersoll, Roxann G.;
Ji Wan Park;
Yah-Huei Wu-Chou;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Beyoung Yun Park;
Sun Ha Jee;
Jabs, Ethylin Wang;
Redett, Richard;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

A novel heterozygous deletion in the EVC2 gene causes Weyers acrofacial dysostosis.

Published in:

Human Genetics, 2006, v. 119, n. 1/2, p. 199, doi. 10.1007/s00439-005-0129-2

By:

Xiaoqian Ye;
Guangtai Song;
Mingwen Fan;
Lisong Shi;
Jabs, Ethylin Wang;
Shangzhi Huang;
Ruiqiang Guo;
Zhuan Bian

Publication type:

Article

Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening.

Published in:

Human Genetics, 2003, v. 114, n. 1, p. 68, doi. 10.1007/s00439-003-1012-7

By:

Cai, Juanliang;
Goodman, Barbara K.;
Patel, Ankita S.;
Mulliken, John B.;
Van Maldergem, Lionel;
Hoganson, George E.;
Paznekas, William A.;
Ben-Neriah, Ziva;
Sheffer, Ruth;
Cunningham, Michael L.;
Daentl, Donna L.;
Jabs, Ethylin Wang

Publication type:

Article

A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Published in:

Human Genetics, 2003, v. 113, n. 1, p. 1, doi. 10.1007/s00439-003-0932-6

By:

Boyadjiev, Simeon A.;
Justice, Cristina M.;
Eyaid, Wafaa;
McKusick, Victor A.;
Lachman, Ralph S.;
Chowdry, Arnab B.;
Jabak, Monzer;
Zwaan, Johan;
Wilson, Alexander F.;
Jabs, Ethylin Wang

Publication type:

Article

Meckel's Cartilage in Mandibular Development and Dysmorphogenesis.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.871927

By:

Pitirri, M. Kathleen;
Durham, Emily L.;
Romano, Natalie A.;
Santos, Jacob I.;
Coupe, Abigail P.;
Zheng, Hao;
Chen, Danny Z.;
Kawasaki, Kazuhiko;
Jabs, Ethylin Wang;
Richtsmeier, Joan T.;
Wu, Meng;
Motch Perrine, Susan M.

Publication type:

Article

Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of FGFR2.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 1, p. 137, doi. 10.1093/hmg/6.1.137

By:

Oldridge, Michael;
Lunt, Peter W.;
Zackai, Elaine H.;
McDonald-McGinn, Donna M.;
Muenke, Maximilian;
Moloney, Dominique M.;
Twigg, Stephen R. F.;
Heath, John K.;
Howard, Timothy D.;
Hoganson, George;
Gagnon, Deborah M.;
Jabs, Ethylin Wang;
Wilkie, Andrew O. M.

Publication type:

Article

Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 7, p. 1229

By:

Park, Woo-Jin;
Meyers, Gregory A.;
Li, Xiang;
Theda, Christiane;
Day, Donald;
Oriow, Seth J.;
Jones, Marilyn C.;
Jabs, Ethylin Wang

Publication type:

Article

Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.

Published in:

2006

By:

Griffith AJ;
Yang Y;
Pryor SP;
Park H;
Jabs EW;
Nadol JB Jr.;
Russell LJ;
Wasserman DI;
Richard G;
Adams JC;
Merchant SN;
Griffith, Andrew J;
Yang, Yandan;
Pryor, Shannon P;
Park, Hong-Joon;
Jabs, Ethylin Wang;
Nadol, Joseph B Jr;
Russell, Laura J;
Wasserman, Daniel I;
Richard, Gabriele

Publication type:

journal article

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion.

Published in:

NPJ Genomic Medicine, 2018, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41525-017-0042-3

By:

Reiner, Jennifer;
Pisani, Laura;
Qiao, Wanqiong;
Singh, Ram;
Yang, Yao;
Shi, Lisong;
Khan, Wahab A.;
Sebra, Robert;
Cohen, Ninette;
Babu, Arvind;
Edelmann, Lisa;
Jabs, Ethylin Wang;
Scott, Stuart A.

Publication type:

Article

Gene expression in pharyngeal arch 1 during human embryonic development.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 7, p. 903, doi. 10.1093/hmg/ddi083

By:

Cai, Juanliang;
Ash, David;
Kotch, Lori E.;
Jabs, Ethylin Wang;
Attie-Bitach, Tania;
Auge, Joelle;
Mattei, Geraldine;
Etchevers, Heather;
Vekemans, Michel;
Korshunova, Yulia;
Tidwell, Rose;
Messina, David N.;
Winston, Julia B.;
Lovett, Michael

Publication type:

Article

Partial Structure and Mapping of the Human Myelin P<sub>2</sub> Protein Gene.

Published in:

Journal of Neurochemistry, 1994, v. 63, n. 6, p. 2010, doi. 10.1046/j.1471-4159.1994.63062010.x

By:

Narayanan, Vinodh;
Ripepi, Benedetta;
Jabs, Ethylin Wang;
Hawkins, Anita;
Griffin, Constance;
Tennekoon, Gihan

Publication type:

Article

Prenatal ultrasonographic and molecular diagnosis of Apert syndrome.

Published in:

1997

By:

Filkins, Karen;
Russo, Joseph F.;
Boehmer, Susan;
Camous, Marianne;
Przylepa, Kelly A.;
Jiang, Wen;
Jabs, Ethylin Wang;
Filkins, K;
Russo, J F;
Boehmer, S;
Camous, M;
Przylepa, K A;
Jiang, W;
Jabs, E W

Publication type:

journal article

Identification of an HMGB3 Frameshift Mutation in a Family With an X-linked Colobomatous Microphthalmia Syndrome Using Whole-Genome and X-Exome Sequencing.

Published in:

JAMA Ophthalmology, 2014, v. 132, n. 10, p. 1215, doi. 10.1001/jamaophthalmol.2014.1731

By:

Scott, Alan F.;
Mohr, David W.;
Kasch, Laura M.;
Barton, Jill A.;
Pittiglio, Raquel;
Ingersoll, Roxann;
Craig, Brian;
Marosy, Beth A.;
Doheny, Kimberly F.;
Bromley, William C.;
Roderick, Thomas H.;
Chassaing, Nicolas;
Calvas, Patrick;
Prabhu, Shreya S.;
Jabs, Ethylin Wang

Publication type:

Article

Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome.

Published in:

Mammalian Genome, 2000, v. 11, n. 11, p. 1000, doi. 10.1007/s003350010193

By:

Norris, Russell A.;
Scott, Karen K.;
Moore, Clara S.;
Stetten, Gail;
Brown, Cuyler R.;
Jabs, Ethylin Wang;
Wulfsberg, Eric A.;
Yu, Jack;
Kern, Michael J.

Publication type:

Article

Cleft Palate in Apert Syndrome.

Published in:

Journal of Developmental Biology, 2022, v. 10, n. 3, p. N.PAG, doi. 10.3390/jdb10030033

By:

Willie, Delayna;
Holmes, Greg;
Jabs, Ethylin Wang;
Wu, Meng

Publication type:

Article

Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex.

Published in:

Journal of Developmental Biology, 2020, v. 8, n. 4, p. 30, doi. 10.3390/jdb8040030

By:

Motch Perrine, Susan M.;
Wu, Meng;
Holmes, Greg;
Bjork, Bryan C.;
Jabs, Ethylin Wang;
Richtsmeier, Joan T.

Publication type:

Article

Universal conditional networks (UniCoN) for multi-age embryonic cartilage segmentation with Sparsely annotated data.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-87797-9

By:

Sapkota, Nishchal;
Zhang, Yejia;
Zhao, Zihao;
Gomez, Maria Jose;
Hsi, Yuhan;
Wilson, Jordan A.;
Kawasaki, Kazuhiko;
Holmes, Greg;
Wu, Meng;
Jabs, Ethylin Wang;
Richtsmeier, Joan T.;
Perrine, Susan M. Motch;
Chen, Danny Z.

Publication type:

Article

Ten-year experience of more than 35,000 orofacial clefts in Africa.

Published in:

BMC Pediatrics, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12887-015-0328-5

By:

Conway, Julia C.;
Taub, Peter J.;
Kling, Rochelle;
Oberoi, Kurun;
Doucette, John;
Jabs, Ethylin Wang

Publication type:

Article

Tyrosine-dependent basolateral targeting of human connexin43–eYFP in Madin–Darby canine kidney cells can be disrupted by the oculodentodigital dysplasia mutation L90V.

Published in:

FEBS Journal, 2009, v. 276, n. 23, p. 6992, doi. 10.1111/j.1742-4658.2009.07407.x

By:

Chtchetinin, Jana;
Gifford, Wes D.;
Li, Sichen;
Paznekas, William A.;
Jabs, Ethylin Wang;
Lai, Albert

Publication type:

Article

Toward understanding the pathogenesis of craniosynostosis through clinical and molecular correlates.

Published in:

Clinical Genetics, 1998, v. 53, n. 2, p. 79, doi. 10.1111/j.1399-0004.1998.tb02648.x

By:

Jabs, Ethylin Wang

Publication type:

Article

Terminal deletion(4)(q33) in a male infant.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 125, doi. 10.1111/j.1399-0004.1982.tb00748.x

By:

Stamberg, Judith;
Jabs, Ethylin Wang;
Elias, Ellen

Publication type:

Article

Embryonic craniofacial bone volume and bone mineral density in Fgfr2<sup>+/P253R</sup> and nonmutant mice.

Published in:

Developmental Dynamics, 2014, v. 243, n. 4, p. 541, doi. 10.1002/dvdy.24095

By:

Percival, Christopher J.;
Huang, Yuan;
Jabs, Ethylin Wang;
Li, Runze;
Richtsmeier, Joan T.

Publication type:

Article

Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.

Published in:

Developmental Dynamics, 2013, v. 242, n. 3, p. C1, doi. 10.1002/dvdy.23940

By:

Martínez‐Abadías, Neus;
Motch, Susan M.;
Pankratz, Talia L.;
Wang, Yingli;
Aldridge, Kristina;
Jabs, Ethylin Wang;
Richtsmeier, Joan T.

Publication type:

Article

Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.

Published in:

Developmental Dynamics, 2013, v. 242, n. 1, p. 80, doi. 10.1002/dvdy.23903

By:

Martínez‐Abadías, Neus;
Motch, Susan M.;
Pankratz, Talia L.;
Wang, Yingli;
Aldridge, Kristina;
Jabs, Ethylin Wang;
Richtsmeier, Joan T.

Publication type:

Article