Friedl W - Search Results

1

Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26.

Caspari R, Uhlhaas S, Friedl W, Knapp M, Propping P. Caspari R, et al. Among authors: friedl w. Am J Med Genet. 2000 Aug 14;93(4):290-3. doi: 10.1002/1096-8628(20000814)93:4<290::aid-ajmg7>3.0.co;2-m. Am J Med Genet. 2000. PMID: 10946355

2

Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.

Faiyaz ul Haque M, Uhlhaas S, Knapp M, Schüler H, Friedl W, Ahmad M, Propping P. Faiyaz ul Haque M, et al. Among authors: friedl w. Hum Genet. 1993 Mar;91(1):17-9. doi: 10.1007/BF00230215. Hum Genet. 1993. PMID: 8454282

3

ADULT syndrome allelic to limb mammary syndrome (LMS)?

Propping P, Friedl W, Wienker TF, Uhlhaas S, Zerres K. Propping P, et al. Among authors: friedl w. Am J Med Genet. 2000 Jan 17;90(2):179-82. Am J Med Genet. 2000. PMID: 10607963

4

MASA syndrome: clinical variability and linkage analysis.

Rietschel M, Friedl W, Uhlhaas S, Neugebauer M, Heimann D, Zerres K. Rietschel M, et al. Among authors: friedl w. Am J Med Genet. 1991 Oct 1;41(1):10-4. doi: 10.1002/ajmg.1320410104. Am J Med Genet. 1991. PMID: 1951449

5

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.

Aretz S, Uhlhaas S, Caspari R, Mangold E, Pagenstecher C, Propping P, Friedl W. Aretz S, et al. Among authors: friedl w. Eur J Hum Genet. 2004 Jan;12(1):52-8. doi: 10.1038/sj.ejhg.5201088. Eur J Hum Genet. 2004. PMID: 14523376

6

Eleven novel germline mutations in the adenomatous polyposis coli (APC) gene.

Paffenholz R, Mandl M, Caspari R, Sengteller M, Propping P, Friedl W. Paffenholz R, et al. Among authors: friedl w. Hum Mol Genet. 1994 Sep;3(9):1703-4. doi: 10.1093/hmg/3.9.1703. Hum Mol Genet. 1994. PMID: 7833936 No abstract available.

7

A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosis.

Mandl M, Kadmon M, Sengteller M, Caspari R, Propping P, Friedl W. Mandl M, et al. Among authors: friedl w. Hum Mol Genet. 1994 Jun;3(6):1009-11. doi: 10.1093/hmg/3.6.1009. Hum Mol Genet. 1994. PMID: 7951213 No abstract available.

8

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.

Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P. Mandl M, et al. Among authors: friedl w. Hum Mol Genet. 1994 Jan;3(1):181-4. doi: 10.1093/hmg/3.1.181. Hum Mol Genet. 1994. PMID: 8162022

9

[Diagnosis of familial adenomatosis polyposis].

Friedl W, Caspari R, Propping P. Friedl W, et al. Dtsch Med Wochenschr. 1994 Jan 7;119(1-2):27-30. doi: 10.1055/s-2008-1058657. Dtsch Med Wochenschr. 1994. PMID: 8281879 Review. German. No abstract available.

10

Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods.

Caspari R, Friedl W, Böker T, Augustin A, Mandl M, Jaeger K, Gallkowski K, Propping P. Caspari R, et al. Among authors: friedl w. Z Gastroenterol. 1993 Nov;31(11):646-52. Z Gastroenterol. 1993. PMID: 8291275

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