Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome

American Journal of Medical Genetics

Volumn 69, Issue 1, 1997, Pages 50-55

  Cuneo, Bettina F ^a,d   Driscoll, Deborah A ^c   Gidding, Samuel S ^b   Langman, Craig B ^b  

^a RUSH MEDICAL COLLEGE   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

^c CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^d ADVOCATE CHRIST MEDICAL CENTER   (United States)

Author keywords

22q11 deletion; chromosomes, human, pair 22; DiGeorge anomaly; heart defects, congenital; hypocalcemic hypoparathyroidism

Indexed keywords

PARATHYROID HORMONE;

ADULT; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; DIGEORGE SYNDROME; FALLOT TETRALOGY; FAMILY STUDY; FEMALE; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; MALE; PARATHYROID HORMONE BLOOD LEVEL; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; EVOLUTION, MOLECULAR; FEMALE; HUMANS; HYPOPARATHYROIDISM; MALE; PEDIGREE; SYNDROME;

EID: 0031046762     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970303)69:1<50::AID-AJMG10>3.0.CO;2-N     Document Type: Article

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