Gross Deletions of the Neurofibromatosis Type 1 (Nf1) Gene Are Predominantly of Maternal Origin and Commonly Associated with a Learning Disability, Dysmorphic Features and Developmental Delay

AuthID
 P-001-7ZV
12
Author(s)
Upadhyaya, M
·
Ruggieri, M
·
Maynard, J
·
Osborn, M
·
Hartog, C
·
Mudd, S
·
Penttinen, M
·
Cordeiro, I
·
Ponder, M
·
Krawczak, M
·
Cooper, DN
Document Type
Article
Year published
1998
Published
in HUMAN GENETICS, ISSN: 0340-6717
Volume: 102, Issue: 5, Pages: 591-597 (7)
Indexing
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Scopus®
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Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 9654211
SCOPUS: 2-s2.0-0031744843
Wos: WOS:000074171100015
Source Identifiers
ISSN: 0340-6717
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