Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations-Reference-Cited by-同舟云学术

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Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations

Published:2002-07-25 Issue:2 Volume:111 Page:205-209
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Engels Hartmut,Bosse Kristin,Ehrbrecht Antje,Zahn Susanne,Hoischen Alexander,Propping Peter,Bindl Lutz,Reutter Heiko

Funder

Deutsche Forschungsgemeinschaft

BONFOR Program of the Medical Faculty of the University of Bonn

Richard-Winter-Stiftung

Doktor-Robert-Pfleger-Stiftung

Nordrhein-Westfalen

Publisher

Wiley

Subject

Genetics (clinical)

Reference20 articles.

1. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes;Bacino;Am J Med Genet,2000

2. A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation;Brackley;Prenat Diagn,1999

3. A distinct osteochondrodysplasia with hypertrichosis: individualization of a probable autosomal recessive entity;Cantú;Hum Genet,1982

4. Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion;Clemens;Am J Med Genet,1996

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