Sanjad Sakati syndrome: A case series from Jordan;Le syndrome de Sanjad-Sakati: Une série de cas en jordanie

Eastern Mediterranean Health Journal

Volumn 18, Issue 5, 2012, Pages 527-531

  Albaramki, J ^a   Akl, K ^a   Al Muhtaseb, A ^a   Al Shboul, M ^b   Mahmoud, T ^b   El Khateeb, M ^b   Hamamy, H ^c  

^a JORDAN UNIVERSITY HOSPITAL   (Jordan)

^b National Center for Diabetes Endocrinology and Genetics Jordan   (Jordan)

^c GENEVA UNIVERSITY HOSPITALS   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE AGE; CHILD; CLINICAL ARTICLE; CONSANGUINITY; CRANIOFACIAL SYNOSTOSIS; EYE DISEASE; EYE EXAMINATION; FEMALE; GENE DELETION; GENETIC SCREENING; GROWTH RETARDATION; HUMAN; HYPERPHOSPHATEMIA; HYPOCALCEMIA; HYPOPARATHYROIDISM; INFANT; INTERVIEW; JORDAN; KIDNEY CALCIFICATION; MALE; MEDICAL RECORD; MENINGITIS; MICROGNATHIA; MORTALITY; PARATHYROID HORMONE BLOOD LEVEL; PHENOTYPIC VARIATION; PHOSPHATE BLOOD LEVEL; PNEUMONIA; SANJAD SAKATI SYNDROME; UREMIA;

EID: 84862313483     PISSN: 10203397     EISSN: None     Source Type: Journal    
DOI: 10.26719/2012.18.5.527     Document Type: Article

References (13)

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