The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation-Reference-Cited by-同舟云学术

The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation

Published:2000-01 Issue:1 Volume:57 Page:83-85
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Devriendt Koenraad,Holvoet Maureen,De Mûelenaere Alain,Fryns Jean-Pierre

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.570113.x/fullpdf

Reference5 articles.

1. Mental retardation with pterygia, shortness and distinct facial appearance: a new MCA/MR syndrome;Haspeslagh;Clin Genet,1985

2. Mental retardation with pterygia, shortness and distinct facial appearance: confirmation of a new MCA/MR syndrome (Letter);Schrander-Stumpel;Clin Genet,1988

3. Haspeslagh syndrome without severe mental retardation and pterygia?;Van Bever;Clin Genet,1995

4. Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH;Delneste;Genet Counsel,1998

5. Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome;Herens;Am J Med Genet,1997

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2. De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalities;American Journal of Medical Genetics;2003-02-21

3. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

4. Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations;American Journal of Medical Genetics;2002-07-25

5. Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation;American Journal of Medical Genetics;2002-01-16