Your browser doesn't support javascript.
loading
Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.
El-Ruby, Mona; El-Din Fayez, Alaa; El-Dessouky, Sara H; Aglan, Mona S; Mazen, Inas; Ismail, Nora; Afifi, Hanan H; Eid, Maha M; Mostafa, Mostafa I; Mehrez, Mennat I; Khalil, Yasmin; Zaki, Maha S; Gaber, Khaled R; Abdel-Hamid, Mohamed S; Abdel-Salam, Ghada M H.
Afiliación
  • El-Ruby M; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • El-Din Fayez A; Medical Molecular Genetics and Enzymology Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • El-Dessouky SH; Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Aglan MS; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Mazen I; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Ismail N; Medical Molecular Genetics and Enzymology Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Afifi HH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Eid MM; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Mostafa MI; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Mehrez MI; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Khalil Y; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Gaber KR; Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Abdel-Hamid MS; Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Abdel-Salam GMH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Am J Med Genet A ; 176(5): 1190-1194, 2018 05.
Article en En | MEDLINE | ID: mdl-29681084
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Factores de Transcripción / Anomalías Craneofaciales / Proteínas de Unión al ADN / Cara / Homocigoto / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child, preschool / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Egipto
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Factores de Transcripción / Anomalías Craneofaciales / Proteínas de Unión al ADN / Cara / Homocigoto / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child, preschool / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Egipto