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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

Author(s)

Upadhyaya, M

Ruggieri, M

Maynard, J

Osborn, M

Hartog, C

Mudd, S

Penttinen, M

Cordeiro, I

Ponder, M

Ponder, BAJ

Krawczak, M

Cooper, DN

Tipo de Documento

Article

Year published

1998

Publicado

in HUMAN GENETICS, ISSN: 0340-6717

Volume: 102, Número: 5, Páginas: 591-597 (7)

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Fontes

Publication Identifiers

DOI: 10.1007/s004390050746

Pubmed: 9654211

SCOPUS: 2-s2.0-0031744843

Wos: WOS:000074171100015

Source Identifiers

ISSN: 0340-6717

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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

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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

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