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Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy.
David, Odeya; Eskin-Schwartz, Marina; Ling, Galina; Dolgin, Vadim; Kristal, Eyal; Benkowitz, Ela; Osyntsov, Lidia; Gradstein, Libe; Birk, Ohad S; Loewenthal, Neta; Yerushalmi, Baruch.
Afiliação
  • David O; Pediatric Endocrinology Unit, Soroka University Medical Center, Beer-Sheva, Israel.
  • Eskin-Schwartz M; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.
  • Ling G; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Dolgin V; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Kristal E; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Benkowitz E; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.
  • Osyntsov L; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Gradstein L; Pediatric Gastroenterology Unit, Soroka University Medical Center, Beer-Sheva, Israel.
  • Birk OS; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Loewenthal N; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.
  • Yerushalmi B; Radiology Department, Soroka Medical Center, Beer-Sheva, Israel.
Clin Genet ; 98(3): 303-307, 2020 09.
Article em En | MEDLINE | ID: mdl-32617964
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipófise / Predisposição Genética para Doença / Peptídeos e Proteínas de Sinalização Intracelular / Ciliopatias Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Israel
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipófise / Predisposição Genética para Doença / Peptídeos e Proteínas de Sinalização Intracelular / Ciliopatias Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Israel