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STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly.
Kakar, Naseebullah; Ahmad, Jamil; Morris-Rosendahl, Deborah J; Altmüller, Janine; Friedrich, Katrin; Barbi, Gotthold; Nürnberg, Peter; Kubisch, Christian; Dobyns, William B; Borck, Guntram.
Affiliation
  • Kakar N; Institute of Human Genetics, University of Ulm, Ulm, Germany.
Hum Genet ; 134(1): 45-51, 2015 Jan.
Article in En | MEDLINE | ID: mdl-25218063
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Holoprosencephaly / Intracellular Signaling Peptides and Proteins / Microcephaly / Mutation Type of study: Etiology_studies Limits: Adolescent / Adult / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2015 Document type: Article Affiliation country: Germany Country of publication: Germany
Fulltext
Add to My VHL
Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Holoprosencephaly / Intracellular Signaling Peptides and Proteins / Microcephaly / Mutation Type of study: Etiology_studies Limits: Adolescent / Adult / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2015 Document type: Article Affiliation country: Germany Country of publication: Germany