Works about HUMAN cytogenetics

Results: 690

Chemically induced premature chromosome condensation in short-term cultured human peripheral lymphocytes: applications to biodosimetry.

Published in:

Biotechnic & Histochemistry, 2007, v. 82, n. 1, p. 29, doi. 10.1080/10520290701257153

By:

Tsuji, S;
Kanda, R

Publication type:

Article

LncRNA ZEB1-AS1 contributes to STAT3 activation by associating with IL-11 in B-lymphoblastic leukemia.

Published in:

Biotechnology Letters, 2017, v. 39, n. 12, p. 1801, doi. 10.1007/s10529-017-2421-3

By:

Wang, Qing;
Du, Xiaoli;
Yang, Min;
Xiao, Shishan;
Cao, Jun;
Song, Jun;
Wang, Linhui

Publication type:

Article

A reappraisal of the significance of largest basal diameter of posterior uveal melanoma.

Published in:

Eye (0950-222X), 2009, v. 23, n. 12, p. 2152, doi. 10.1038/eye.2009.235

By:

Damato, B.;
Coupland, S. E.

Publication type:

Article

OP08.01: Cytogenetic analysis in fetuses with late onset abnormal sonographic findings.

Published in:

Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 71, doi. 10.1002/uog.17761

By:

Bardin, R.;
Hadar, E.;
Meizner, I.;
Basel-Vanagaite, L.;
Haizler-Cohen, L.;
Wiznitzer, A.;
Maya, I.

Publication type:

Article

Prenatal diagnosis of a cleidocranial dysplasia-like phenotype associated with a de novo balanced t(2q;6q)(q36;q16) translocation.

Published in:

Ultrasound in Obstetrics & Gynecology, 2003, v. 22, n. 6, p. 648, doi. 10.1002/uog.916

By:

Winer, N.;
Le Caigneci, C.;
Quere, M. P.;
David, A.;
Boceno, M.;
Aubron, F.;
Joubert, M.;
Boog, G.;
Philippe, H. J.;
Rival, J. M.

Publication type:

Article

Variations in the Phagosomal Environment of Human Neutrophils and Mononuclear Phagocyte Subsets.

Published in:

Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00188

By:

Foote, Juliet R.;
Patel, Amit A.;
Yona, Simon;
Segal, Anthony W.

Publication type:

Article

Jumping Translocations of 1q in Myelodysplastic Syndrome and Acute Myeloid Leukemia: Report of Three Cases and Review of Literature.

Published in:

2018

By:

Couture, T.;
Amato, K.;
DiAdamo, A.;
Li, P.

Publication type:

Case Study

Use of primed in situ labeling (PRINS) for the detection of telomeric deletions associated with mental retardation.

Published in:

Cytogenetics & Cell Genetics, 2001, v. 93, n. 1/2, p. 16, doi. 10.1159/000056939

By:

Bonifacio, S.;
Centrone, C.;
Da Prato, L.;
Scordo, M. R.;
Estienne, M.;
Torricelli, F.

Publication type:

Article

Erratum.

Published in:

2001

By:

Li, Y. -C.;
Lee, C.;
Hseu, T. -H.;
Li, S. -Y.;
Lin, C. C.

Publication type:

Erratum

A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).

Published in:

Cytogenetics & Cell Genetics, 2000, v. 91, n. 1-4, p. 85, doi. 10.1159/000056824

By:

Dufke, A.;
Eggermann, K.;
Balg, S.;
Stengel-Rutkowski, S.;
Enders, H.;
Kaiser, P.

Publication type:

Article

The long-term effect of external quality assessment on performance in service cytogenetics.

Published in:

Cytogenetics & Cell Genetics, 2000, v. 91, n. 1-4, p. 124, doi. 10.1159/000056831

By:

Held, K. R.;
Eiben, B.;
Miny, P.

Publication type:

Article

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Published in:

Cytogenetics & Cell Genetics, 2000, v. 91, n. 1-4, p. 165, doi. 10.1159/000056839

By:

Levy, B.;
Papenhausen, P. R.;
Tepperberg, J. H.;
Dunn, T. M.;
Fallet, S.;
Magid, M. S.;
Kardon, N. B.;
Hirschhorn, K.;
Warburton, P. E.

Publication type:

Article

Familial mosaicism of del(Y) and inv del(Y).

Published in:

Cytogenetics & Cell Genetics, 2000, v. 91, n. 1-4, p. 208, doi. 10.1159/000056846

By:

Röttger, S.;
Pasantes, J. J.;
Baldermann, C.;
Reichl, E.;
Yen, P. H.;
Hansmann, I.;
Schempp, W.

Publication type:

Article

Discrepancies in cytogenetic results between different tissues in two fetuses with Wolf- Hirschhorn syndrome.

Published in:

Cytogenetics & Cell Genetics, 2000, v. 91, n. 1-4, p. 231, doi. 10.1159/000056850

By:

Schinzel, A.

Publication type:

Article

Congenital acute lymphoblastic leukemia: a two-case report and a review of the literature.

Published in:

2011

By:

Suárez, Ma Pilar Bas;
Brito, Jezabel López;
Reyes, Candelaria Santana;
Muñoz, Manuel Gresa;
Pulido, Rosario Diaz;
Rojas, Jose Carlos Lodos;
Bas Suárez, Maria Pilar;
López Brito, Jezabel;
Santana Reyes, Candelaria;
Gresa Muñoz, Manuel;
Diaz Pulido, Rosario;
Lodos Rojas, Jose Carlos

Publication type:

journal article

Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism.

Published in:

2010

By:

Jenderny, Jutta;
Schmidt, Winfried;
Bartsch, Oliver

Publication type:

journal article

Mongolism Preventable by Amniocentesis.

Published in:

Clinical Pediatrics, 1971, v. 10, n. 10, p. 554, doi. 10.1177/000992287101001003

By:

Bodensteiner, J. B.;
Zellweger, H.

Publication type:

Article

FAMILIAL MONGOLISM.

Published in:

Clinical Pediatrics, 1964, v. 3, n. 5, p. 291, doi. 10.1177/000992286400300510

By:

Zellweger, Hans

Publication type:

Article

Gene copy number variation in male breast cancer by aCGH.

Published in:

Analytical Cellular Pathology: Cellular Oncology, 2010, v. 33, n. 3/4, p. 113, doi. 10.1155/2010/468280

By:

Tommasi, Stefania;
Mangia, Anita;
Iannelli, Giuseppina;
Chiarappa, Patrizia;
Rossi, Elena;
Ottini, Laura;
Mottolese, Marcella;
Zoli, Wainer;
Zuffardi, Orsetta;
Paradiso, Angelo

Publication type:

Article

Felix A. Conte, MD, 1935–2024: The Endocrinologist's Endocrinologist.

Published in:

2025

By:

Miller, Walter L.;
Rosenthal, Stephen M.;
Gitelman, Stephen E.;
Lustig, Robert H.;
Styne, Dennis M.

Publication type:

Obituary

Chromosomal Aberrations Associated with Clonal Evolution and Leukemic Transformation in Fanconi Anemia: Clinical and Biological Implications.

Published in:

Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/349837

By:

Meyer, Stefan;
Neitzel, Heidemarie;
Tonnies, Holger

Publication type:

Article

Gestational, perinatal and family findings of patients with Patau syndrome.

Published in:

Revista Paulista de Pediatria, 2013, v. 31, n. 4, p. 459, doi. 10.1590/s0103-05822013000400007

By:

Rosa, Rafael Fabiano M.;
Vaz Sarmento, Melina;
Borges Polli, Janaina;
de Paoli Groff, Daniela;
Petry, Patrícia;
de Mattos, Vinícius Freitas;
Rosa, Rosana Cardoso M.;
Trevisan, Patrícia;
Zen, Paulo Ricardo G.

Publication type:

Article

Systematic Screening for Subtelomeric Anomalies in a Clinical Sample of Autism.

Published in:

Journal of Autism & Developmental Disorders, 2007, v. 37, n. 4, p. 703, doi. 10.1007/s10803-006-0196-9

By:

Wassink, Thomas H.;
Losh, Molly;
Piven, Joseph;
Sheffield, Val C.;
Ashley, Elizabeth;
Westin, Erik R.;
Patil, Shivanand R.

Publication type:

Article

Medical Cytogenetics (Book).

Published in:

1967

By:

Mellman, William J.

Publication type:

Book Review

Prevalencia de alteraciones cromosómicas en pacientes infértiles estudiadas en una clínica de reproducción asistida.

Published in:

Ginecología y Obstetricia de México, 2009, v. 77, n. 3, p. 128

By:

Tovar, Sergio Romero;
Espinosa, Berenice Juárez;
García, Carlos G. Galindo;
Romo, Margarita Mendoza;
Usabiaga, Rafael A. Sánchez

Publication type:

Article

An Emerging 1q21.1 Deletion-Associated Neurodevelopmental Phenotype.

Published in:

Journal of Child Neurology, 2011, v. 26, n. 1, p. 113, doi. 10.1177/0883073810377658

By:

Basel-Vanagaite, Lina;
Goldberg-Stern, Hadassa;
Mimouni-Bloch, Aviva;
Shkalim, Vered;
Böhm, Detlef;
Kohlhase, Jürgen

Publication type:

Article

Asiaticoside induces osteogenic differentiation of human periodontal ligament cells through the Wnt pathway.

Published in:

2018

By:

Fitri, Atika Resti;
Pavasant, Prasit;
Chamni, Supakarn;
Sumrejkanchanakij, Piyamas

Publication type:

journal article

The genetics of autism.

Published in:

Acta Psychiatrica Scandinavica, 2001, v. 103, n. 6, p. 411, doi. 10.1034/j.1600-0447.2001.00086.x

By:

Lauritsen, M.;
Ewald, H.

Publication type:

Article

Genetic abnormalities in Turkish women with premature ovarian failure

Published in:

2010

By:

Ceylaner, Gulay;
Altinkaya, Sunduz Ozlem;
Mollamahmutoglu, Leyla;
Ceylaner, Serdar

Publication type:

journal article

Osteoclast diseases.

Published in:

Microscopy Research & Technique, 2003, v. 61, n. 6, p. 514, doi. 10.1002/jemt.10375

By:

Miep H. Helfrich

Publication type:

Article

Molecular Analysis of Pediatric Oligodendrogliomas Highlights Genetic Differences with Adult Counterparts and Other Pediatric Gliomas.

Published in:

Brain Pathology, 2016, v. 26, n. 2, p. 206, doi. 10.1111/bpa.12291

By:

Nauen, David;
Haley, Lisa;
Lin, Ming‐Tseh;
Perry, Arie;
Giannini, Caterina;
Burger, Peter C.;
Rodriguez, Fausto J.

Publication type:

Article

Nodule Formation and Desmoplasia in Medulloblastomas—Defining the Nodular/Desmoplastic Variant and Its Biological Behavior.

Published in:

Brain Pathology, 2007, v. 17, n. 2, p. 151, doi. 10.1111/j.1750-3639.2007.00058.x

By:

McManamy, Charles S.;
Pears, Jane;
Weston, Claire L.;
Hanzely, Zoltan;
Ironside, James W.;
Taylor, Roger E.;
Grundy, Richard G.;
Clifford, Steven C.;
Ellison, David W.

Publication type:

Article

Epilepsy and the new cytogenetics.

Published in:

Epilepsia (Series 4), 2011, v. 52, n. 3, p. 423, doi. 10.1111/j.1528-1167.2010.02932.x

By:

Mulley, John C.;
Mefford, Heather C.

Publication type:

Article

Pediatric Sclerosing Rhabdomyosarcoma.

Published in:

International Journal of Surgical Pathology, 2006, v. 14, n. 3, p. 193, doi. 10.1177/1066896906290558

By:

Zambrano, Eduardo;
Pérez-Atayde, Antonio R.;
Ahrens, William;
Reyes-Mügica, Miguel

Publication type:

Article

Human Cytomegalovirus and Colorectal Adenocarcinoma: Any Association?

Published in:

Iraqi Journal of Medical Sciences, 2008, v. 6, n. 2, p. 54

By:

Baqer Al-Obaidi, Asmaa'

Publication type:

Article

DETECTION OF A 12P13 CHROMOSOME ANOMALY INVOLVING ETV6 AT RELAPSE IN AN ADOLESCENT PRESENTING WITH CYTOGENETICALLY NORMAL, FLT3-ITD<sup>+</sup>, TYPE A NPM1<sup>+</sup> DE NOVO AML (M5 FAB-TYPE).

Published in:

Ulster Medical Journal, 2009, v. 78, n. 1, p. 71

By:

McGrattan, P.;
Humphreys, M. W.;
Mills, K. I.;
Gilkes, A. F.;
McMullin, M. F.

Publication type:

Article

A 5Q DELETION WITH A CRYPTIC ETV6/RUNX1 IN A CASE OF CHILDHOOD ALL.

Published in:

Ulster Medical Journal, 2009, v. 78, n. 1, p. 71

By:

McNerlan, S. E.;
McGrattan, P.;
Cairns, C.;
Dempsey, S. I.;
Humphreys, M. W.

Publication type:

Article

ABNORMALITIES OF 3Q26 IN MYELOID MALIGNANCY: THE BELFAST EXPERIENCE.

Published in:

Ulster Medical Journal, 2009, v. 78, n. 1, p. 69

By:

McNerlan, S. E.;
McGrattan, P.;
Logan, A.;
Humphreys, M.

Publication type:

Article

Exposición a Solventes Orgánicos y Efectos Genotóxicos en Trabajadores de Fábricas de Pinturas en Bogotá.

Published in:

Revista de Salud Pública, 2007, v. 9, n. 2, p. 275

By:

Cárdenas-Bustamante, Omayda;
Varona-Uribe, Marcela;
Patiño-Florez, Rosa I.;
Groot-Restrepo, Helena;
Sicard-Suárez, Diana;
Tórres-Carvajal, Maria M.;
Pardo-Pardo, Darío

Publication type:

Article

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies.

Published in:

Jornal de Pediatria, 2015, v. 91, n. 2, p. 189, doi. 10.1016/j.jpedp.2014.07.007

By:

Lay-Son, Guillermo;
Espinoza, Karena;
Vial, Cecilia;
Rivera, Juan C.;
Guzmán, María L.;
Repetto, Gabriela M.

Publication type:

Article

History of Science & Technology.

Published in:: 2009
Publication type:: Abstract

Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.

Published in:

Congenital Anomalies, 2006, v. 46, n. 2, p. 115, doi. 10.1111/j.1741-4520.2006.00111.x

By:

Kosaki, Rika;
Hanai, Sae;
Kakishima, Hiroki;
Okada, Michiyo A.;
Hayashi, Satoshi;
Ito, Yushi;
Takahashi, Takao;
Kosaki, Kenjiro;
Okuyama, Torayuki

Publication type:

Article

Primena fluorescentne in situ hibridizacije u hematologiji.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2012, v. 69, n. 11, p. 986, doi. 10.2298/VSP1211986M

By:

Milošević, Ivana;
Popović, Stevan;
Urošević, Ivana

Publication type:

Article

Cytogenetic findings in pediatric radiation-induced atypical meningioma after treatment of medulloblastoma: case report and review of the literature.

Published in:

Journal of Neuro-Oncology, 2012, v. 110, n. 3, p. 397, doi. 10.1007/s11060-012-0982-5

By:

Brassesco, María;
Valera, Elvis;
Neder, Luciano;
Pezuk, Julia;
Oliveira, Ricardo;
Scrideli, Carlos;
Tone, Luiz

Publication type:

Article

Hyperdiploidy defines a distinct cytogenetic entity of meningiomas.

Published in:

Journal of Neuro-Oncology, 2007, v. 83, n. 2, p. 213

By:

Yoo-Jin Kim;
Simone Storck;
Jörg Rahnenführer;
Bernd Romeike;
Wolf-Ingo Steudel;
Klaus Zang;
Wolfram Henn

Publication type:

Article

Expression and subcellular localization of syntaxin 11 in human neutrophils.

Published in:

Inflammation Research, 2009, v. 58, n. 7, p. 407

By:

Janis de la Iglesia-Vicente;
Yun-xiang Fang;
Faustino Mollinedo

Publication type:

Article

In vitro effect of fenthion on human lymphocytes.

Published in:

Bulletin of Environmental Contamination & Toxicology, 1991, v. 47, n. 2, p. 316, doi. 10.1007/BF01688658

By:

Usha Rani, M.;
Rao, M.

Publication type:

Article

Molecular cytogenetic diagnosis in 591 married couples with reproductive failures: application for genetic counseling, IVF and PGD.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 20, p. S26, doi. 10.1016/S1472-6483(10)62326-7

By:

Vorsanova, S. G.;
Beresheva, A. K.;
Demidova, I. A.;
Iourov, I. Y.;
Kolotii, A. D.;
Kravetz, V. S.;
Kurinnaya, O.;
Yurov, Y. B.

Publication type:

Article

Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of Oman.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2009, v. 18, n. 3, p. 424, doi. 10.1016/S1472-6483(10)60104-6

By:

Goud, Tadakal Mallana;
Harassi, Salma Mohammed Al;
Salmani, Kamla Khalfan Al;
Busaidy, Suleiman Mohammed Al;
Rajab, Anna

Publication type:

Article

Preimplantation genetic testing outcomes for poor prognosis cryptic translocation carrier couples.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, p. S-44

By:

N., Ercelen;
E., Tutar;
M., Gultomruk;
B., Balaban;
C., Alatas;
K., Yakin;
B., Urman

Publication type:

Article