Rappold GA - Search Results

1

Physical mapping of 14 new DNA markers isolated from the human distal Xp region.

Wapenaar MC, Petit C, Basler E, Ballabio A, Henke A, Rappold GA, van Paassen HM, Blonden LA, van Ommen GJ. Wapenaar MC, et al. Among authors: rappold ga. Genomics. 1992 May;13(1):167-75. doi: 10.1016/0888-7543(92)90217-g. Genomics. 1992. PMID: 1349572

2

Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomere.

Henke A, Fischer C, Rappold GA. Henke A, et al. Among authors: rappold ga. Genomics. 1993 Dec;18(3):478-85. doi: 10.1016/s0888-7543(11)80003-0. Genomics. 1993. PMID: 8307556

3

Arrangement and localization of the human GM-CSF receptor alpha chain gene CSF2RA within the X-Y pseudoautosomal region.

Rappold G, Willson TA, Henke A, Gough NM. Rappold G, et al. Genomics. 1992 Oct;14(2):455-61. doi: 10.1016/s0888-7543(05)80241-1. Genomics. 1992. PMID: 1358805

4

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.

Henke A, Wapenaar M, van Ommen GJ, Maraschio P, Camerino G, Rappold G. Henke A, et al. Am J Hum Genet. 1991 Oct;49(4):811-9. Am J Hum Genet. 1991. PMID: 1897527 Free PMC article.

5

AK1 detects a VNTR locus in the pseudoautosomal region.

Klink A, Wapenaar M, van Ommen GJ, Rappold G. Klink A, et al. Hum Mol Genet. 1993 Mar;2(3):339. doi: 10.1093/hmg/2.3.339-a. Hum Mol Genet. 1993. PMID: 8098983 No abstract available.

6

PA2.1 detects a TaqI polymorphism in the pseudoautosomal region.

Henke A, Rappold G. Henke A, et al. Hum Mol Genet. 1993 Mar;2(3):339. doi: 10.1093/hmg/2.3.339. Hum Mol Genet. 1993. PMID: 8098984 No abstract available.

7

High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).

Wang I, Franco B, Ferrero GB, Chinault AC, Weissenbach J, Chumakov I, Le Paslier D, Levilliers J, Klink A, Rappold GA, Ballabio A, Petit C. Wang I, et al. Among authors: rappold ga. Genomics. 1995 Mar 20;26(2):229-38. doi: 10.1016/0888-7543(95)80205-z. Genomics. 1995. PMID: 7601447

8

A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy.

Franco B, Meroni G, Parenti G, Levilliers J, Bernard L, Gebbia M, Cox L, Maroteaux P, Sheffield L, Rappold GA, Andria G, Petit C, Ballabio A. Franco B, et al. Among authors: rappold ga. Cell. 1995 Apr 7;81(1):15-25. doi: 10.1016/0092-8674(95)90367-4. Cell. 1995. PMID: 7720070 Free article.

9

Characterization of a YAC contig spanning the pseudoautosomal region.

Ried K, Mertz A, Nagaraja R, Trusgnich M, Riley JH, Anand R, Lehrach H, Page D, Ellison JW, Rappold G. Ried K, et al. Genomics. 1995 Oct 10;29(3):787-92. doi: 10.1006/geno.1995.9933. Genomics. 1995. PMID: 8575778

10

Chromosomal localisation of a pseudoautosomal growth gene(s).

Ogata T, Petit C, Rappold G, Matsuo N, Matsumoto T, Goodfellow P. Ogata T, et al. J Med Genet. 1992 Sep;29(9):624-8. doi: 10.1136/jmg.29.9.624. J Med Genet. 1992. PMID: 1404292 Free PMC article.

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