Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion-Reference-Cited by-同舟云学术

Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion

Published:2011-12 Issue:4 Volume:50 Page:506-511
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,Su Yi-Ning,Chen Yi-Yung,Su Jun-Wei,Chern Schu-Rern,Chen Yu-Ting,Chen Wen-Lin,Chen Li-Feng,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference22 articles.

1. Defizien an den kurzen Armen eines Chromosoms Nr 4;Wolf;Humangenetik,1965

2. Deletion of short arms of chromosome 4–5 in a child with defects of midline fusion;Hirschhorn;Humangenetik,1965

3. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision;Battaglia;Am J Med Genet C Semin Med Genet,2008

4. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review;Zollino;Am J Med Genet C Semin Med Genet,2008

5. WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma;Stec;Hum Mol Genet,1998

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1. Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations;Taiwanese Journal of Obstetrics and Gynecology;2024-03

2. A case of inversion of chromosome 4 and an unbalanced transloca- tion between the short arm of chromosome 4 and long arm of chromosome 18 in a girl: evolution of clinical and electroencephalographic manifestations;Russian Journal of Child Neurology;2021-02-26

3. Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene;Molecular Cytogenetics;2021-02-24

4. Wolf–Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly;Taiwanese Journal of Obstetrics and Gynecology;2020-05

5. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones;Taiwanese Journal of Obstetrics and Gynecology;2017-12