Literature DB >> 3772677

Absence of parathyroid tissue in sex-linked recessive hypoparathyroidism.

M P Whyte, G S Kim, M Kosanovich.   

Abstract

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Year:  1986        PMID： 3772677     DOI： 10.1016/s0022-3476(86)80741-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  9 in total

Review 1.  Molecular genetics of mineral metabolic disorders.

Authors:  R V Thakker
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 2.  Gene mapping of mineral metabolic disorders.

Authors:  R V Thakker; K E Davies; J L O'Riordan
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

3.  Male triplets concordant for X-linked recessive nonsyndromic hypoparathyroidism.

Authors:  A S Teebi; A R Kishawi; A H Malek
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

4.  Craniofacioskeletal syndrome: an X-linked dominant disorder with early lethality in males.

Authors:  Roger E Stevenson; Cam K Brasington; Cindy Skinner; Richard J Simensen; J Edward Spence; Shelli Kesler; Allan L Reiss; Charles E Schwartz
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802

5.  Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Authors:  D Trump; P H Dixon; S Mumm; C Wooding; K E Davies; D Schlessinger; M P Whyte; R V Thakker
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

6.  mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.

Authors:  S Mumm; M P Whyte; R V Thakker; K H Buetow; D Schlessinger
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

7.  The functional burden of diabetic retinopathy in the United States.

Authors:  Dipal Nagda; William Mitchell; Nazlee Zebardast
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2021-04-29       Impact factor: 3.117

8.  Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.

Authors:  R V Thakker; K E Davies; M P Whyte; C Wooding; J L O'Riordan
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

9.  An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.

Authors:  Michael R Bowl; M Andrew Nesbit; Brian Harding; Elaine Levy; Andrew Jefferson; Emanuela Volpi; Karine Rizzoti; Robin Lovell-Badge; David Schlessinger; Michael P Whyte; Rajesh V Thakker
Journal:  J Clin Invest       Date:  2005-09-15       Impact factor: 14.808
  9 in total

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