Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly-Reference-Cited by-同舟云学术

Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly

Published:2011-06 Issue:2 Volume:50 Page:182-187
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Kuo Yau-Kun,Su Yi-Ning,Chern Schu-Rern,Tsai Fuu-Jen,Wu Pei-Chen,Chen Yu-Ting,Town Dai-Dyi,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference24 articles.

1. Isochromosome 18q in a fetus with congenital megacystis, intrauterine growth retardation and cloacal dysgenesis sequence;Chen;Prenat Diagn,1998

2. Isochromosome 18q with karyotype 46, XX, i(18q). Cytogenetics and pathology;Froster-Iskenius;Clin Genet,1984

3. Prenatal diagnosis of a congenital anomaly of isochromosome 18q—a case report;Shyu;Clin Med J,1988

4. Chromosomal abnormalities in fetuses with omphalocele: significance of omphalocele contents;Nyberg;J Ultrasound Med,1989

5. Holoprosencephaly in a newborn girl with 46, XX, i(18q). Holoprosencephaly in a newborn girl with 46, XX, i(18q);Spinner;Am J Med Genet,1991

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