Propping P - Search Results

1

Genetic counseling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection.

Kruse R, Guttenbach M, Schartmann B, Schubert R, van der Ven H, Schmid M, Propping P. Kruse R, et al. Among authors: propping p. Fertil Steril. 1998 Mar;69(3):482-5. doi: 10.1016/s0015-0282(97)00539-6. Fertil Steril. 1998. PMID: 9531882 Free article.

2

[Skin diseases and genetic instability. II. Genetic dermatoses with genetic instability].

Kruse R, Propping P. Kruse R, et al. Among authors: propping p. Hautarzt. 1998 Feb;49(2):W153-63. doi: 10.1007/s001050050721. Hautarzt. 1998. PMID: 9551344 Review. German. No abstract available.

3

Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients.

Friedl W, Kruse R, Uhlhaas S, Stolte M, Schartmann B, Keller KM, Jungck M, Stern M, Loff S, Back W, Propping P, Jenne DE. Friedl W, et al. Among authors: propping p. Genes Chromosomes Cancer. 1999 Aug;25(4):403-6. Genes Chromosomes Cancer. 1999. PMID: 10398437

4

[Skin diseases and genetic instability. I: Basic principles of genetic instability].

Kruse R, Propping P. Kruse R, et al. Among authors: propping p. Hautarzt. 1998 Jan;49(1):65-71. doi: 10.1007/s001050050704. Hautarzt. 1998. PMID: 9522197 Review. German. No abstract available.

5

A gene for universal congenital alopecia maps to chromosome 8p21-22.

Nöthen MM, Cichon S, Vogt IR, Hemmer S, Kruse R, Knapp M, Höller T, Faiyaz ul Haque M, Haque S, Propping P, Ahmad M, Rietschel M. Nöthen MM, et al. Among authors: propping p. Am J Hum Genet. 1998 Feb;62(2):386-90. doi: 10.1086/301717. Am J Hum Genet. 1998. PMID: 9463324 Free PMC article.

6

A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among Europeans.

Wang Y, Friedl W, Lamberti C, Nöthen MM, Kruse R, Propping P. Wang Y, et al. Among authors: propping p. Hum Hered. 1998 Mar-Apr;48(2):87-91. doi: 10.1159/000022786. Hum Hered. 1998. PMID: 9526167

7

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.

Cichon S, Kruse R, Hillmer AM, Kukuk G, Anker M, Altland K, Knapp M, Propping P, Nöthen MM. Cichon S, et al. Among authors: propping p. Br J Dermatol. 2000 Oct;143(4):811-4. doi: 10.1046/j.1365-2133.2000.03781.x. Br J Dermatol. 2000. PMID: 11069461

8

Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue.

Wang Y, Friedl W, Lamberti C, Ruelfs C, Kruse R, Propping P. Wang Y, et al. Among authors: propping p. Hum Genet. 1997 Sep;100(3-4):362-4. doi: 10.1007/s004390050517. Hum Genet. 1997. PMID: 9272156

9

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.

Cichon S, Anker M, Vogt IR, Rohleder H, Pützstück M, Hillmer A, Farooq SA, Al-Dhafri KS, Ahmad M, Haque S, Rietschel M, Propping P, Kruse R, Nöthen MM. Cichon S, et al. Among authors: propping p. Hum Mol Genet. 1998 Oct;7(11):1671-9. doi: 10.1093/hmg/7.11.1671. Hum Mol Genet. 1998. PMID: 9736769

10

Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.

Wehner M, Buschhausen L, Lamberti C, Kruse R, Caspari R, Propping P, Friedl W. Wehner M, et al. Among authors: propping p. Hum Mutat. 1997;10(3):241-4. doi: 10.1002/(SICI)1098-1004(1997)10:3<241::AID-HUMU12>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9298827 No abstract available.

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