Jansen S - Search Results

1

Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.

Gibson RA, Ford D, Jansen S, Savoia A, Havenga C, Milner RD, de Ravel TJ, Cohn RJ, Ball SE, Roberts I, et al. Gibson RA, et al. Among authors: jansen s. J Med Genet. 1994 Nov;31(11):868-71. doi: 10.1136/jmg.31.11.868. J Med Genet. 1994. PMID: 7853372 Free PMC article.

2

Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.

Pronk JC, Gibson RA, Savoia A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Ortega JJ, Jansen S, et al. Pronk JC, et al. Among authors: jansen s. Nat Genet. 1995 Nov;11(3):338-40. doi: 10.1038/ng1195-338. Nat Genet. 1995. PMID: 7581462

3

Novel mutations and polymorphisms in the Fanconi anemia group C gene.

Gibson RA, Morgan NV, Goldstein LH, Pearson IC, Kesterton IP, Foot NJ, Jansen S, Havenga C, Pearson T, de Ravel TJ, Cohn RJ, Marques IM, Dokal I, Roberts I, Marsh J, Ball S, Milner RD, Llerena JC Jr, Samochatova E, Mohan SP, Vasudevan P, Birjandi F, Hajianpour A, Murer-Orlando M, Mathew CG. Gibson RA, et al. Among authors: jansen s. Hum Mutat. 1996;8(2):140-8. doi: 10.1002/(SICI)1098-1004(1996)8:2<140::AID-HUMU6>3.0.CO;2-F. Hum Mutat. 1996. PMID: 8844212

4

Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa.

Tipping AJ, Pearson T, Morgan NV, Gibson RA, Kuyt LP, Havenga C, Gluckman E, Joenje H, de Ravel T, Jansen S, Mathew CG. Tipping AJ, et al. Among authors: jansen s. Proc Natl Acad Sci U S A. 2001 May 8;98(10):5734-9. doi: 10.1073/pnas.091402398. Proc Natl Acad Sci U S A. 2001. PMID: 11344308 Free PMC article.

5

Positional cloning of the Fanconi anaemia group A gene.

Fanconi anaemia/Breast cancer consortium. Fanconi anaemia/Breast cancer consortium. Nat Genet. 1996 Nov;14(3):324-8. doi: 10.1038/ng1196-324. Nat Genet. 1996. PMID: 8896564

6

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.

Faivre L, Guardiola P, Lewis C, Dokal I, Ebell W, Zatterale A, Altay C, Poole J, Stones D, Kwee ML, van Weel-Sipman M, Havenga C, Morgan N, de Winter J, Digweed M, Savoia A, Pronk J, de Ravel T, Jansen S, Joenje H, Gluckman E, Mathew CG. Faivre L, et al. Among authors: jansen s. Blood. 2000 Dec 15;96(13):4064-70. Blood. 2000. PMID: 11110674 Free article.

7

Fanconi anemia. a statistical evaluation of cytogenetic results obtained from South African families.

Pearson T, Jansen S, Havenga C, Stones DK, Joubert G. Pearson T, et al. Among authors: jansen s. Cancer Genet Cytogenet. 2001 Apr 1;126(1):52-5. doi: 10.1016/s0165-4608(00)00388-5. Cancer Genet Cytogenet. 2001. PMID: 11343779

8

A common Fanconi anemia mutation in black populations of sub-Saharan Africa.

Morgan NV, Essop F, Demuth I, de Ravel T, Jansen S, Tischkowitz M, Lewis CM, Wainwright L, Poole J, Joenje H, Digweed M, Krause A, Mathew CG. Morgan NV, et al. Among authors: jansen s. Blood. 2005 May 1;105(9):3542-4. doi: 10.1182/blood-2004-10-3968. Epub 2005 Jan 18. Blood. 2005. PMID: 15657175 Free article.

9

Clinical studies of multiple endocrine neoplasia type 1 (MEN1).

Trump D, Farren B, Wooding C, Pang JT, Besser GM, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Monson JP, O'Halloran D, Sampson J, Shalet SM, Wheeler MH, Zink A, Thakker RV. Trump D, et al. Among authors: jansen s. QJM. 1996 Sep;89(9):653-69. doi: 10.1093/qjmed/89.9.653. QJM. 1996. PMID: 8917740

10

[Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].

Himmelmann A, Bortoluzzi L, Jansen S, Fehr J. Himmelmann A, et al. Among authors: jansen s. Schweiz Med Wochenschr. 2000 Aug 8;130(31-32):1112-9. Schweiz Med Wochenschr. 2000. PMID: 11008304 German.

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