Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX-Reference-Cited by-同舟云学术

Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX

Published:2001 Issue:2 Volume:102 Page:192-199
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Sutcliffe Maxine J.,Mueller O. Thomas,Kousseff Boris G.,Dumont Doris P.,McFarland Julia A.,Mawani Fayaz,Conforto Danielle,Ranells Judith D.

Publisher

Wiley

Subject

Genetics(clinical)

Reference44 articles.

1. Isochromosome 18p in a mother and her child

2. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3)

3. 18q− and 18q+ mosaicism in a mentally retarded boy

4. Partial Trisomy of Chromosome 18 (pter→q12) following a Familial 18;21 Translocation rcp(18;21)(q12;q11)

5. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.

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1. Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report;Molecular Cytogenetics;2008-11-11

2. Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving Structural and Numerical Abnormalities of Chromosome 18;Journal of Histochemistry & Cytochemistry;2007-07-11

3. 46,XY,18q+/46,XY,18q− mosaicism in a fragile X prenatal diagnosis;Prenatal Diagnosis;2005

4. A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation;American Journal of Medical Genetics Part A;2005

5. Identification and Molecular Characterization of a de novo Supernumerary Ring Chromosome 18 in a Patient with Klippel-Trenaunay Syndrome;Annals of Human Genetics;2004-07