The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies

Clinical Dysmorphology

Volumn 6, Issue 3, 1997, Pages 233-237

  Al Gazali, L I ^a   Dawodu, A ^a  

^a UNITED ARAB EMIRATES UNIVERSITY   (United Arab Emirates)

Author keywords

Arabs; Autosomal recessive; Developmental delay; Hypoparathyroidism

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CLINICAL FEATURE; FACIES; GENETIC LINKAGE; GROWTH RETARDATION; HUMAN; HYPOPARATHYROIDISM; INFANT; MALE; PRIORITY JOURNAL;

CONSANGUINITY; DEVELOPMENTAL DISABILITIES; FACE; FEMALE; GENES, RECESSIVE; GROWTH DISORDERS; HUMANS; HYPOPARATHYROIDISM; INFANT; MALE; PHENOTYPE; SYNDROME;

EID: 0030835292     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199707000-00006     Document Type: Article

References (14)

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