Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome

Clin Genet. 2010 Apr;77(4):404-7. doi: 10.1111/j.1399-0004.2009.01355.x. Epub 2010 Jan 20.

Authors

J F Mazzeu¹, A M Vianna-Morgante, A C V Krepischi, A Oudakker, C Rosenberg, K Szuhai, J McGill, J Maccraughan, H van Bokhoven, H G Brunner

Affiliation

¹ Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, Brazil.

PMID: 20095987
DOI: 10.1111/j.1399-0004.2009.01355.x

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / diagnosis
Abnormalities, Multiple / diagnostic imaging
Abnormalities, Multiple / genetics*
Abnormalities, Multiple / pathology*
Child
Child, Preschool
Chromosome Breakage
Chromosome Deletion*
Chromosomes, Human, Pair 1 / genetics*
Female
Genes, Dominant / genetics*
Humans
Infant
Male
Radiography
Syndrome