Read AP - Search Results

1

A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.

Hughes AE, Newton VE, Liu XZ, Read AP. Hughes AE, et al. Among authors: read ap. Nat Genet. 1994 Aug;7(4):509-12. doi: 10.1038/ng0894-509. Nat Genet. 1994. PMID: 7951321

2

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.

Tassabehji M, Read AP, Newton VE, Patton M, Gruss P, Harris R, Strachan T. Tassabehji M, et al. Among authors: read ap. Nat Genet. 1993 Jan;3(1):26-30. doi: 10.1038/ng0193-26. Nat Genet. 1993. PMID: 8490648

3

Waardenburg syndrome.

Read AP, Newton VE. Read AP, et al. J Med Genet. 1997 Aug;34(8):656-65. doi: 10.1136/jmg.34.8.656. J Med Genet. 1997. PMID: 9279758 Free PMC article. Review.

4

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

Foy C, Newton V, Wellesley D, Harris R, Read AP. Foy C, et al. Among authors: read ap. Am J Hum Genet. 1990 Jun;46(6):1017-23. Am J Hum Genet. 1990. PMID: 2339698 Free PMC article.

5

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.

Liu XZ, Newton VE, Read AP. Liu XZ, et al. Among authors: read ap. Am J Med Genet. 1995 Jan 2;55(1):95-100. doi: 10.1002/ajmg.1320550123. Am J Med Genet. 1995. PMID: 7702105 Review.

6

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

Tassabehji M, Newton VE, Read AP. Tassabehji M, et al. Among authors: read ap. Nat Genet. 1994 Nov;8(3):251-5. doi: 10.1038/ng1194-251. Nat Genet. 1994. PMID: 7874167

7

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse.

Tassabehji M, Newton VE, Leverton K, Turnbull K, Seemanova E, Kunze J, Sperling K, Strachan T, Read AP. Tassabehji M, et al. Among authors: read ap. Hum Mol Genet. 1994 Jul;3(7):1069-74. doi: 10.1093/hmg/3.7.1069. Hum Mol Genet. 1994. PMID: 7981674

8

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.

Tassabehji M, Read AP, Newton VE, Harris R, Balling R, Gruss P, Strachan T. Tassabehji M, et al. Among authors: read ap. Nature. 1992 Feb 13;355(6361):635-6. doi: 10.1038/355635a0. Nature. 1992. PMID: 1347148

9

Localization of a gene for Waardenburg syndrome type I.

Read AP, Foy C, Newton V, Harris R. Read AP, et al. Ann N Y Acad Sci. 1991;630:143-51. doi: 10.1111/j.1749-6632.1991.tb19583.x. Ann N Y Acad Sci. 1991. PMID: 1952585 No abstract available.

10

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Van Camp G, Van Thienen MN, Handig I, Van Roy B, Rao VS, Milunsky A, Read AP, Baldwin CT, Farrer LA, Bonduelle M, et al. Van Camp G, et al. Among authors: read ap. J Med Genet. 1995 Jul;32(7):531-6. doi: 10.1136/jmg.32.7.531. J Med Genet. 1995. PMID: 7562965 Free PMC article.

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