Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency

Journal of Clinical Endocrinology and Metabolism

Volumn 91, Issue 11, 2006, Pages 4510-4513

  Porzio, Ottavia ^a   Cunsolo, V ^a   Malaponti, M ^a   De Nisco, E ^a   Acquafredda, A ^d   Cavallo, L ^d   Andreani, M ^b   Giardina, E ^a   Testi, M ^b   Cappa, M ^c   Federici, G ^a,c  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

^b Immunogenetics Laboratory   (Italy)

^c BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^d UNIVERSITY OF BARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

HLA ANTIGEN;

ARTICLE; CASE REPORT; CHROMOSOME MUTATION; CONGENITAL ADRENAL HYPERPLASIA; DNA HYBRIDIZATION; FEMALE; GENE CONVERSION; GENE SEQUENCE; GENETIC RECOMBINATION; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; MALE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SIBLING; SOUTHERN BLOTTING; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 33751506699     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2006-0779     Document Type: Article

References (20)

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