Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/32923
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Type: Journal article
Title: Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome
Author: Villard, L.
Fontes, M.
Ades, L.
Gecz, J.
Citation: American Journal of Medical Genetics Part A, 2000; 91(1):83-85
Publisher: Wiley-Liss
Issue Date: 2000
ISSN: 1552-4825
1552-4833
Statement of
Responsibility: 
Laurent Villard, Michel Fontès, Lesley C. Adès, Jozef Gecz
Keywords: Face
Humans
Microcephaly
Abnormalities, Multiple
Syndrome
DNA Helicases
Nuclear Proteins
DNA
Pedigree
DNA Mutational Analysis
Sequence Deletion
Base Sequence
Sequence Homology, Nucleic Acid
Mutation
Frameshift Mutation
Point Mutation
Family Health
Female
Male
Intellectual Disability
Description: Letter to the Editor
Rights: © 2000 Wiley-Liss, Inc.
DOI: 10.1002/(SICI)1096-8628(20000306)91:1<83::AID-AJMG15>3.3.CO;2-E
Published version: http://dx.doi.org/10.1002/(sici)1096-8628(20000306)91:1%3C83::aid-ajmg15%3E3.0.co;2-n
Appears in Collections:Aurora harvest
Paediatrics publications

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