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HESX1: a novel gene implicated in a familial form of septo-optic dysplasia.
Dattani, M T; Martinez-Barbera, J P; Thomas, P Q; Brickman, J M; Gupta, R; Wales, J K; Hindmarsh, P C; Beddington, R S; Robinson, I C.
Affiliation
  • Dattani MT; London Centre for Paediatric Endocrinology and Metabolism, Institute of Child Health, UK. m.dattani@ich.ucl.ac.uk
Acta Paediatr Suppl ; 88(433): 49-54, 1999 Dec.
Article in En | MEDLINE | ID: mdl-10626545
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Collection: 01-internacional Database: MEDLINE Main subject: Septum Pellucidum / Genes, Homeobox / Helix-Loop-Helix Motifs / Homeodomain Proteins Limits: Animals / Humans Language: En Journal: Acta Paediatr Suppl Year: 1999 Document type: Article Affiliation country: Reino Unido Country of publication: Noruega
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Septum Pellucidum / Genes, Homeobox / Helix-Loop-Helix Motifs / Homeodomain Proteins Limits: Animals / Humans Language: En Journal: Acta Paediatr Suppl Year: 1999 Document type: Article Affiliation country: Reino Unido Country of publication: Noruega