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Items: 14

1.

Mutations in the Gs alpha gene causing hormone resistance.

Mantovani G, Spada A.

Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):501-13. Review.

PMID:
17161328
2.

GNAS locus and pseudohypoparathyroidism.

Bastepe M, J├╝ppner H.

Horm Res. 2005;63(2):65-74. Epub 2005 Feb 9. Review.

3.

Pseudo-pseudohypoparathyroidism.

ALBRIGHT F, FORBES AP, HENNEMAN PH.

Trans Assoc Am Physicians. 1952;65:337-50. No abstract available.

PMID:
13005676
4.
6.

Imprinting in Albright's hereditary osteodystrophy.

Davies SJ, Hughes HE.

J Med Genet. 1993 Feb;30(2):101-3. Review.

7.

Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.

Wilson LC, Oude Luttikhuis ME, Clayton PT, Fraser WD, Trembath RC.

J Med Genet. 1994 Nov;31(11):835-9.

8.

Albright's hereditary osteodystrophy: a review.

Fitch N.

Am J Med Genet. 1982 Jan;11(1):11-29. Review. No abstract available.

PMID:
6278930
9.

Pseudohypoparathyroidism: inheritance of deficient receptor-cyclase coupling activity.

Farfel Z, Brothers VM, Brickman AS, Conte F, Neer R, Bourne HR.

Proc Natl Acad Sci U S A. 1981 May;78(5):3098-102.

10.

Autosomal dominant inheritance in Albright's hereditary osteodystrophy.

Weinberg AG, Stone RT.

J Pediatr. 1971 Dec;79(6):996-9. No abstract available.

PMID:
5125407
11.

Pseudohypoparathyroidism: defective excretion of 3',5'-AMP in response to parathyroid hormone.

Chase LR, Melson GL, Aurbach GD.

J Clin Invest. 1969 Oct;48(10):1832-44.

12.

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.

Weinstein LS, Gejman PV, Friedman E, Kadowaki T, Collins RM, Gershon ES, Spiegel AM.

Proc Natl Acad Sci U S A. 1990 Nov;87(21):8287-90.

13.

Pseudohypoparathyroidism. Variable manifestations within a family.

Williams AJ, Wilkinson JL, Taylor WH.

Arch Dis Child. 1977 Oct;52(10):798-800.

14.

Pseudohypoparathyroidism: report on a family with four affected sisters.

Kinard RE, Walton JE, Buckwalter JA.

Arch Intern Med. 1979 Feb;139(2):204-7.

PMID:
219790
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