Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay-Reference-Cited by-同舟云学术

Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay

Published:2006 Issue:5 Volume:140A Page:488-495
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Weimer Jörg,Metzke-Heidemann Simone,Plendl Hansjörg,Caliebe Almuth,Grunewald Regina,Õunap Katrin,Tammur Pille,Jonat Walter,Bartsch Oliver,Siebert Reiner,Arnold Norbert

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. Detailed characterization of 12 supernumerary ring chromosomes using micro‐FISH and search for uniparental disomy

2. Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11

3. Mitotic and meiotic behaviour of a naturally transmitted ring Y chromosome: reproductive risk evaluation

4. FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy

5. Preferential involvement of the short arm in chromosome 8-derived supernumerary markers and ring as identified by chromosome arm painting

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3. Another Small Supernumerary Marker Chromosome Derived from Chromosome 9 in a Klinefelter Patient;West Indian Medical Journal;2012-12

4. Neural bases of childhood speech disorders: Lateralization and plasticity for speech functions during development;Neuroscience & Biobehavioral Reviews;2012-01

5. Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes;Molecular Syndromology;2012