Literature DB >> 5308088

Congenital familial hypoparathyroidism. Management of an infant, genetics, pathogenesis of hypoparathyroidism, and fetal undermineralization.

R Gorodischer, T Aceto, K Terplan.   

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Year:  1970        PMID： 5308088

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  2 in total

1.  Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus.

Authors:  A G Hunter; H Heick; W J Poznanski; P N McLaine
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

2.  Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.

Authors:  R Parvari; E Hershkovitz; A Kanis; R Gorodischer; S Shalitin; V C Sheffield; R Carmi
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025
  2 in total

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