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CLASS RECITATION IN INSURANCE.
Published in:
Journal of Education, 1919, v. 89, n. 25, p. 686, doi. 10.1177/002205741908902503
By:
- Shaffer, L. G.
Publication type:
Article
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.
Published in:
Clinical Genetics, 2008, v. 74, n. 5, p. 469, doi. 10.1111/j.1399-0004.2008.01094.x
By:
- Ballif, B. C.;
- Theisen, A.;
- McDonald-McGinn, D. M.;
- Zackai, E. H.;
- Hersh, J. H.;
- Bejjani, B. A.;
- Shaffer, L. G.
Publication type:
Article
Silver-Russell syndrome and exclusion of uniparental disomy.
Published in:
Clinical Genetics, 1996, v. 50, n. 6, p. 494, doi. 10.1111/j.1399-0004.1996.tb02720.x
By:
- Ayala-Madrigal, M. L.;
- Shaffer, L. G.;
- Ramírez-Dueñas, M. L.
Publication type:
Article
Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus-Merzbacher disease.
Published in:
2001
By:
- Inoue, K;
- Kanai, M;
- Tanabe, Y;
- Kubota, T;
- Kashork, C D;
- Wakui, K;
- Fukushima, Y;
- Lupski, J R;
- Shaffer, L G
Publication type:
journal article
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridization.
Published in:
1999
By:
- Kashork, Catherine D.;
- Lupski, James R.;
- Shaffer, Lisa G.;
- Kashork, C D;
- Lupski, J R;
- Shaffer, L G
Publication type:
journal article
ANALYSIS OF NINE PREGNANCIES WITH CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2.
Published in:
Prenatal Diagnosis, 1996, v. 16, n. 10, p. 899, doi. 10.1002/(SICI)1097-0223(199610)16:10<899::AID-PD960>3.0.CO;2-M
By:
- SHAFFER, L. G.;
- LANGLOIS, S.;
- McCASKILL, C.;
- MAIN, D. M.;
- ROBINSON, W. P.;
- BARRETT, I. J.;
- KALOUSEK, D. K.
Publication type:
Article
Mosaicism for trisomy 12: four cases with varying outcomes.
Published in:
1995
By:
- Bischoff, Farideh Z.;
- Zenger-Hain, Julie;
- Moses, David;
- van Dyke, Daniel L.;
- Shaffer, Lisa G.;
- Bischoff, F Z;
- Zenger-Hain, J;
- Moses, D;
- Van Dyke, D L;
- Shaffer, L G
Publication type:
journal article
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism.
Published in:
1995
By:
- Jones, Carrie;
- Booth, Carol;
- Rita, Debra;
- Jazmines, Lydia;
- Spiro, Rhonda;
- McCulloch, Brian;
- McCaskill, Christopher;
- Shaffer, Lisa G.;
- Jones, C;
- Booth, C;
- Rita, D;
- Jazmines, L;
- Spiro, R;
- McCulloch, B;
- McCaskill, C;
- Shaffer, L G
Publication type:
journal article
Prenatal ultrasound findings in a fetus with paternal uniparental disomy 14q12-qter.
Published in:
Ultrasound in Obstetrics & Gynecology, 2001, v. 18, n. 3, p. 268, doi. 10.1046/j.1469-0705.2001.00451.x
By:
- Towner, D.;
- Yang, S. P.;
- Shaffer, L. G.
Publication type:
Article
Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvement.
Published in:
2001
By:
- Inoue, Ken;
- Tanaka, Hajime;
- Scaglia, Fernando;
- Araki, Akiko;
- Shaffer, Lisa G.;
- Lupski, James R.;
- Inoue, K;
- Tanaka, H;
- Scaglia, F;
- Araki, A;
- Shaffer, L G;
- Lupski, J R
Publication type:
journal article
Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia.
Published in:
Leukemia (08876924), 2011, v. 25, n. 6, p. 1042, doi. 10.1038/leu.2011.33
By:
- Yu, L.;
- Slovak, M. L.;
- Mannoor, K.;
- Chen, C.;
- Hunger, S. P.;
- Carroll, A. J.;
- Schultz, R. A.;
- Shaffer, L. G.;
- Ballif, B. C.;
- Ning, Y.
Publication type:
Article
A dual-color FISH assay distinguishes between ELL and MLLT1 (ENL) gene rearrangements in t(11;19)-positive acute leukemia.
Published in:
Leukemia (08876924), 2006, v. 20, n. 11, p. 2046, doi. 10.1038/sj.leu.2404371
By:
- Biggerstaff, J. S.;
- Liu, W.;
- Slovak, M. L.;
- Bobadilla, D.;
- Bryant, E.;
- Glotzbach, C.;
- Shaffer, L. G.
Publication type:
Article
Nomenclature Evolution: Changes in the ISCN from the 2005 to the 2009 Edition.
Published in:
Cytogenetic & Genome Research, 2010, v. 127, n. 1, p. 1, doi. 10.1159/000279442
By:
- Brothman, A. R.;
- Persons, D. L.;
- Shaffer, L. G.
Publication type:
Article
Medical applications of array CGH and the transformation of clinical cytogenetics.
Published in:
Cytogenetic & Genome Research, 2006, v. 115, n. 3/4, p. 303, doi. 10.1159/000095928
By:
- Shaffer, L. G.;
- Bejjani, B. A.
Publication type:
Article
Rearrangements of chromosome 18 illustrate the utility of array-based comparative genomic hybridization.
Published in:
Cytogenetic & Genome Research, 2006, v. 114, n. 3/4, p. 379, doi. 10.1159/000094228
By:
- C. D.Kashork;
- Theisen, A.;
- Bejjani, B. A.;
- Shaffer, L. G.
Publication type:
Article
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly.
Published in:
Molecular Syndromology, 2013, v. 3, n. 6, p. 247, doi. 10.1159/000345578
By:
- Rosenfeld, J. A.;
- Kim, K. H.;
- Angle, B.;
- Troxell, R.;
- Gorski, J. L.;
- Westemeyer, M.;
- Frydman, M.;
- Senturias, Y.;
- Earl, D.;
- Torchia, B.;
- Schultz, R. A.;
- Ellison, J. W.;
- Tsuchiya, K.;
- Zimmerman, S.;
- Smolarek, T. A.;
- Ballif, B. C.;
- Shaffer, L. G.
Publication type:
Article
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions.
Published in:
Molecular Syndromology, 2012, v. 3, n. 3, p. 102, doi. 10.1159/000342008
By:
- Traylor, R. N.;
- Dobyns, W. B.;
- Rosenfeld, J. A.;
- Wheeler, P.;
- Spence, J. E.;
- Bandholz, A. M.;
- Bawle, E. V.;
- Carmany, E. P.;
- Powell, C. M.;
- Hudson, B.;
- Schultz, R. A.;
- Shaffer, L. G.;
- Ballif, B. C.
Publication type:
Article

Found: 17