X-linked hypophosphatemia: A search for gender, race, anticipation, or parent of origin effects on disease expression in children

Journal of Clinical Endocrinology and Metabolism

Volumn 81, Issue 11, 1996, Pages 4075-4080

  Whyte, Michael P ^a   Schranck, Francine W ^b   Armamento Villareal, Reina ^b  

^a SHRINERS HOSPITAL FOR CHILDREN   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHATE;

ARTICLE; CAUCASIAN; FEMALE; GENE DOSAGE; GENETIC HETEROGENEITY; GLOMERULUS FILTRATION RATE; HUMAN; MAJOR CLINICAL STUDY; MALE; MINERAL BALANCE; NEGRO; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SEX LINKAGE; VITAMIN D RESISTANT RICKETS;

AFRICAN CONTINENTAL ANCESTRY GROUP; BODY HEIGHT; CHILD; CHILD, PRESCHOOL; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE EXPRESSION; GENES, DOMINANT; HUMANS; HYPOPHOSPHATEMIA; KIDNEY; LINKAGE (GENETICS); MALE; PARENTS; PHOSPHATES; SEX CHARACTERISTICS; X CHROMOSOME;

GLOMERULUS; PIERINAE;

EID: 0029798574     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.81.11.4075     Document Type: Article

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