Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18

M. H. Lee; S. Y. Park; Y. M. Kim; J. M. Kim; J. Y. Han; M. Y. Kim; H. M. Ryu

doi:10.1002/pd.224

Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18

Prenatal Diagnosis ◽

10.1002/pd.224 ◽

2002 ◽

Vol 22 (2) ◽

pp. 102-104 ◽

Cited By ~ 7

Author(s):

M. H. Lee ◽

S. Y. Park ◽

Y. M. Kim ◽

J. M. Kim ◽

J. Y. Han ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Chromosomal Rearrangement ◽

Complex Chromosomal Rearrangement

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Prenatal Diagnosis of 2q32 Deletion Syndrome Characterized by Multiple Segmental Deletions and Complex Chromosomal Rearrangement Involving Chromosomes 2, 5 and 7

Fetal Diagnosis and Therapy ◽

10.1159/000335650 ◽

2012 ◽

Vol 31 (3) ◽

pp. 196-200 ◽

Cited By ~ 1

Author(s):

Heidi L. Thorson ◽

Urvashi Surti ◽

Malini Sathanoori ◽

Sally J. Kochmar ◽

Beth Torchia ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Chromosomal Rearrangement ◽

Deletion Syndrome ◽

Complex Chromosomal Rearrangement

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Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3–7p15.3, including TWIST1 gene – a case report

Ginekologia Polska ◽

10.17772/gp/1768 ◽

2014 ◽

Vol 85 (7) ◽

Cited By ~ 4

Author(s):

Diana Massalska ◽

Julia Bijok ◽

Anna Kucińska-Chahwan ◽

Aleksander Jamsheer ◽

Joanna Bogdanowicz ◽

...

Keyword(s):

Case Report ◽

Prenatal Diagnosis ◽

Chromosomal Rearrangement ◽

De Novo ◽

Complex Chromosomal Rearrangement

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Prenatal diagnosis of ade novo complex chromosomal rearrangement involving four chromosomes

Prenatal Diagnosis ◽

10.1002/pd.1970060308 ◽

1986 ◽

Vol 6 (3) ◽

pp. 211-216 ◽

Cited By ~ 16

Author(s):

Hyon Ju Kim ◽

Mary Ann Perle ◽

Virginia Bogosian ◽

Alba Greco

Keyword(s):

Prenatal Diagnosis ◽

Chromosomal Rearrangement ◽

Complex Chromosomal Rearrangement

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A Complex Chromosomal Rearrangement Involving 46,XX,t(1;7;16)(p32.1;q22;q13) in a Female with Recurrent Miscarriages Afterin vitroFertilization

Laboratory Medicine Online ◽

10.3343/lmo.2013.3.3.178 ◽

2013 ◽

Vol 3 (3) ◽

pp. 178

Author(s):

Hanjoon Kim ◽

Juwon Kim ◽

Young Uh ◽

Kap Jun Yoon ◽

Hyuck Dong Han

Keyword(s):

Chromosomal Rearrangement ◽

Recurrent Miscarriages ◽

Complex Chromosomal Rearrangement

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Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studies

Scientific Reports ◽

10.1038/srep39760 ◽

2017 ◽

Vol 7 (1) ◽

Cited By ~ 5

Author(s):

Aurélie Mouka ◽

Vincent Izard ◽

Gérard Tachdjian ◽

Sophie Brisset ◽

Frank Yates ◽

...

Keyword(s):

Stem Cell ◽

Pluripotent Stem Cell ◽

Chromosomal Rearrangement ◽

Genetic Model ◽

Induced Pluripotent Stem Cell ◽

Cell Generation ◽

Complex Chromosomal Rearrangement ◽

Induced Pluripotent

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A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity

Journal of Medical Genetics ◽

10.1136/jmg.37.11.892 ◽

2000 ◽

Vol 37 (11) ◽

pp. 892-896

Author(s):

W. EMBERGER

Keyword(s):

Early Onset ◽

Chromosomal Rearrangement ◽

De Novo ◽

Complex Chromosomal Rearrangement

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An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype

European Journal of Medical Genetics ◽

10.1016/j.ejmg.2006.10.007 ◽

2007 ◽

Vol 50 (2) ◽

pp. 133-138 ◽

Cited By ~ 23

Author(s):

Iris Bartels ◽

Heike Starke ◽

Loukas Argyriou ◽

Simone M. Sauter ◽

Barbara Zoll ◽

...

Keyword(s):

Chromosomal Rearrangement ◽

Normal Phenotype ◽

Complex Chromosomal Rearrangement

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Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication ofSIX1,SIX6, andOTX2resulting from a complex chromosomal rearrangement

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.32398 ◽

2008 ◽

Vol 146A (19) ◽

pp. 2480-2489 ◽

Cited By ~ 26

Author(s):

Zhishuo Ou ◽

Donna M. Martin ◽

Jirair K. Bedoyan ◽

M. Lance Cooper ◽

A. Craig Chinault ◽

...

Keyword(s):

Chromosomal Rearrangement ◽

Complex Chromosomal Rearrangement ◽

Oculoauriculovertebral Spectrum

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Multicolour FISH fine mapping unravels an insertion as a complex chromosomal rearrangement involving six breakpoints and a 5.89 Mb large deletion

Journal of Medical Genetics ◽

10.1136/jmg.40.5.e60 ◽

2003 ◽

Vol 40 (5) ◽

pp. 60e-60 ◽

Cited By ~ 2

Author(s):

J Kraus

Keyword(s):

Fine Mapping ◽

Chromosomal Rearrangement ◽

Large Deletion ◽

Complex Chromosomal Rearrangement ◽

Multicolour Fish

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A new human natural killer leukemia cell line, IMC-1. A complex chromosomal rearrangement defined by spectral karyotyping: functional and cytogenetic characterization

Leukemia Research ◽

10.1016/s0145-2126(03)00254-6 ◽

2004 ◽

Vol 28 (3) ◽

pp. 275-284 ◽

Cited By ~ 11

Author(s):

I-Ming Chen ◽

Margaret Whalen ◽

Arthur Bankhurst ◽

Cordelia E Sever ◽

Rashmi Doshi ◽

...

Keyword(s):

Natural Killer ◽

Cell Line ◽

Chromosomal Rearrangement ◽

Leukemia Cell ◽

Leukemia Cell Line ◽

Spectral Karyotyping ◽

Complex Chromosomal Rearrangement ◽

Cytogenetic Characterization

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