Yates J - Search Results

1

Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

Jouet M, Feldman E, Yates J, Donnai D, Paterson J, Siggers D, Kenwrick S. Jouet M, et al. Among authors: yates j. J Med Genet. 1993 Mar;30(3):214-7. doi: 10.1136/jmg.30.3.214. J Med Genet. 1993. PMID: 8474107 Free PMC article.

2

Linkage analysis in 16 families with incontinentia pigmenti.

Jouet M, Stewart H, Landy S, Yates J, Yong SL, Harris A, Garret C, Hatchwell E, Read A, Donnai D, Kenwrick S. Jouet M, et al. Among authors: yates j. Eur J Hum Genet. 1997 May-Jun;5(3):168-70. Eur J Hum Genet. 1997. PMID: 9272741

3

Nine novel L1 CAM mutations in families with X-linked hydrocephalus.

MacFarlane JR, Du JS, Pepys ME, Ramsden S, Donnai D, Charlton R, Garrett C, Tolmie J, Yates JR, Berry C, Goudie D, Moncla A, Lunt P, Hodgson S, Jouet M, Kenwrick S. MacFarlane JR, et al. Among authors: yates jr. Hum Mutat. 1997;9(6):512-8. doi: 10.1002/(SICI)1098-1004(1997)9:6<512::AID-HUMU3>3.0.CO;2-3. Hum Mutat. 1997. PMID: 9195224

4

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Zhang Y, McMahon R, Charles SJ, Green JS, Moore AT, Barton DE, Yates JR. Zhang Y, et al. Among authors: yates jr. J Med Genet. 1993 Nov;30(11):923-5. doi: 10.1136/jmg.30.11.923. J Med Genet. 1993. PMID: 8301646 Free PMC article.

5

Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

Yates JR, Warner JP, Smith JA, Deymeer F, Azulay JP, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Affara NA, Ferguson-Smith MA. Yates JR, et al. J Med Genet. 1993 Feb;30(2):108-11. doi: 10.1136/jmg.30.2.108. J Med Genet. 1993. PMID: 8445613 Free PMC article.

6

Improved genetic mapping of X linked retinoschisis.

George ND, Payne SJ, Bill RM, Barton DE, Moore AT, Yates JR. George ND, et al. Among authors: yates jr. J Med Genet. 1996 Nov;33(11):919-22. doi: 10.1136/jmg.33.11.919. J Med Genet. 1996. PMID: 8950671 Free PMC article.

7

Genetic mapping of X linked ocular albinism: linkage analysis in British families.

Charles SJ, Moore AT, Yates JR. Charles SJ, et al. Among authors: yates jr. J Med Genet. 1992 Aug;29(8):552-4. doi: 10.1136/jmg.29.8.552. J Med Genet. 1992. PMID: 1355560 Free PMC article.

8

Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers.

Maher ER, Bentley E, Payne SJ, Latif F, Richards FM, Chiano M, Hosoe S, Yates JR, Linehan M, Barton DE, et al. Maher ER, et al. Among authors: yates jr. J Med Genet. 1992 Dec;29(12):902-5. doi: 10.1136/jmg.29.12.902. J Med Genet. 1992. PMID: 1362224 Free PMC article.

9

Chimaerism shown by cytogenetics and DNA polymorphism analysis.

Green AJ, Barton DE, Jenks P, Pearson J, Yates JR. Green AJ, et al. Among authors: yates jr. J Med Genet. 1994 Oct;31(10):816-7. doi: 10.1136/jmg.31.10.816. J Med Genet. 1994. PMID: 7837260 Free PMC article.

10

Bootstrapping in human genetic linkage.

Chiano MN, Yates JR. Chiano MN, et al. Among authors: yates jr. Ann Hum Genet. 1994 May;58(2):129-43. doi: 10.1111/j.1469-1809.1994.tb01882.x. Ann Hum Genet. 1994. PMID: 7979157

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