Interstitial deletion 2p11.2-p12: Further delineation

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 149A; no. 10; pp. 2324 - 2326
Main Authors Writzl, Karin, Lovrečić, Luca, Peterlin, Borut
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.10.2009
Wiley-Liss
Subjects
Abnormalities, Multiple - genetics
Biological and medical sciences
Child
Chromosome Deletion
Chromosomes, Human, Pair 2
Gait Ataxia - complications
Gait Ataxia - genetics
Humans
Language Development Disorders - complications
Language Development Disorders - genetics
Lower Extremity Deformities, Congenital - complications
Lower Extremity Deformities, Congenital - genetics
Male
Medical genetics
Medical sciences
Motor Skills Disorders - complications
Motor Skills Disorders - genetics
Chromosomal aberration
Deletion
Symptomatology
Phenotype
Interstitial
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Bibliography:istex:99F74113BAE316831AEBE46EAC2E859249063B33
ArticleID:AJMG33064
ark:/67375/WNG-X2BRPR7T-4
How to cite this article: Writzl K, Lovrečić L, Peterlin B. 2009. Interstitial deletion 2p11.2-p12: Further delineation. Am J Med Genet Part A 149A:2324-2326.
How to cite this article: Writzl K, Lovrečić L, Peterlin B. 2009. Interstitial deletion 2p11.2–p12: Further delineation. Am J Med Genet Part A 149A:2324–2326.
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.33064