Your browser doesn't support javascript.
loading
Sanjad-Sakati syndrome in a Tunisian child.
Kerkeni, E; Sakka, R; Sfar, S; Bouaziz, S; Ghedira, N; Ben Ameur, K; Ben Hmida, H; Chioukh, F-Z; Ghédira, E S; Gribaa, M; Monastiri, K.
Afiliação
  • Kerkeni E; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of intensive care and neonatal medicine, CHU Fattouma Bourguiba, Monastir, Tunisia. Electronic address: emnakerkeni@gmail.com.
  • Sakka R; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of intensive care and neonatal medicine, CHU Fattouma Bourguiba, Monastir, Tunisia.
  • Sfar S; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia.
  • Bouaziz S; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia.
  • Ghedira N; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia.
  • Ben Ameur K; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of intensive care and neonatal medicine, CHU Fattouma Bourguiba, Monastir, Tunisia.
  • Ben Hmida H; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of intensive care and neonatal medicine, CHU Fattouma Bourguiba, Monastir, Tunisia.
  • Chioukh FZ; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of intensive care and neonatal medicine, CHU Fattouma Bourguiba, Monastir, Tunisia.
  • Ghédira ES; Laboratory of biology, CHU Fattouma Bourguiba, Monastir, Tunisia.
  • Gribaa M; Laboratory of human cytogenetics, molecular genetics and reproductive biology, Farhat Hached University Hospital, Sousse, Tunisia.
  • Monastiri K; Research Unit 01/UR/08-14, Faculty of medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of intensive care and neonatal medicine, CHU Fattouma Bourguiba, Monastir, Tunisia.
Arch Pediatr ; 22(9): 951-5, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26231322
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Convulsões / Anormalidades Múltiplas / Recém-Nascido Prematuro / Éxons / Chaperonas Moleculares / Face / Transtornos do Crescimento / Hipoparatireoidismo / Deficiência Intelectual Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Newborn País/Região como assunto: Africa Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Convulsões / Anormalidades Múltiplas / Recém-Nascido Prematuro / Éxons / Chaperonas Moleculares / Face / Transtornos do Crescimento / Hipoparatireoidismo / Deficiência Intelectual Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Newborn País/Região como assunto: Africa Idioma: En Ano de publicação: 2015 Tipo de documento: Article