Literature DB >> 6018993

Pigmentary disorders in association with congenital deafness.

W B Reed, V M Stone, E Boder, L Ziprkowski.   

Abstract

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Mesh：

Year:  1967        PMID： 6018993

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN： 0003-987X


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  12 in total

Review 1.  Waardenburg syndrome.

Authors:  A P Read; V E Newton
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

Review 2.  Hirschsprung's disease as a neurochristopathy.

Authors:  G Martucciello
Journal:  Pediatr Surg Int       Date:  1997       Impact factor: 1.827

3.  Waardenburg syndrome type 2.

Authors:  Subhash Chandra Shaw; Shekhar Neema; Amit Devgan; Rakesh Maggon
Journal:  Med J Armed Forces India       Date:  2017-07-17

4.  Homozygosity in piebald trait.

Authors:  M A Hultén; M M Honeyman; A J Mayne; M J Tarlow
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

5.  Feline hereditary neuroaxonal dystrophy.

Authors:  J C Woodard; G H Collins; J R Hessler
Journal:  Am J Pathol       Date:  1974-03       Impact factor: 4.307

6.  Dominant piebald trait (white forelock and leukoderma) with neurological impairment.

Authors:  M A Telfer; M Sugar; E A Jaeger; J Mulcahy
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025

7.  Pigment distribution in Waardenburg's syndrome: a new hypothesis.

Authors:  T M Nork; Z M Shihab; R S Young; J Price
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1986       Impact factor: 3.117

8.  Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.

Authors:  Y Shiloh; G Litvak; Y Ziv; T Lehner; L Sandkuyl; M Hildesheimer; V Buchris; F P Cremers; P Szabo; B N White
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

9.  Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors:  C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

Review 10.  Heterogeneity in Waardenburg syndrome.

Authors:  M J Hageman; J W Delleman
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025
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