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Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.
Uz, Elif; Alanay, Yasemin; Aktas, Dilek; Vargel, Ibrahim; Gucer, Safak; Tuncbilek, Gokhan; von Eggeling, Ferdinand; Yilmaz, Engin; Deren, Ozgur; Posorski, Nicole; Ozdag, Hilal; Liehr, Thomas; Balci, Sevim; Alikasifoglu, Mehmet; Wollnik, Bernd; Akarsu, Nurten A.
Affiliation
  • Uz E; Gene Mapping Laboratory, Department of Medical Genetics, Hacettepe University Medical Faculty, Sihhiye, Ankara, Turkey.
Am J Hum Genet ; 86(5): 789-96, 2010 May 14.
Article in En | MEDLINE | ID: mdl-20451171
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Microphthalmos / Cleft Palate / Homeodomain Proteins / Musculoskeletal Abnormalities / Mutation Type of study: Etiology_studies / Prognostic_studies Limits: Humans Language: En Journal: Am J Hum Genet Year: 2010 Type: Article Affiliation country: Turkey
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Microphthalmos / Cleft Palate / Homeodomain Proteins / Musculoskeletal Abnormalities / Mutation Type of study: Etiology_studies / Prognostic_studies Limits: Humans Language: En Journal: Am J Hum Genet Year: 2010 Type: Article Affiliation country: Turkey