Krebsova A - Search Results

1

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

Zielenski J, Corey M, Rozmahel R, Markiewicz D, Aznarez I, Casals T, Larriba S, Mercier B, Cutting GR, Krebsova A, Macek M Jr, Langfelder-Schwind E, Marshall BC, DeCelie-Germana J, Claustres M, Palacio A, Bal J, Nowakowska A, Ferec C, Estivill X, Durie P, Tsui LC. Zielenski J, et al. Among authors: krebsova a. Nat Genet. 1999 Jun;22(2):128-9. doi: 10.1038/9635. Nat Genet. 1999. PMID: 10369249 No abstract available.

2

Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival.

Macek M Jr, Macek M Sr, Krebsová A, Nash E, Hamosh A, Reis A, Varon-Mateeva R, Schmidtke J, Maestri NE, Sperling K, Krawczak M, Cutting GR. Macek M Jr, et al. Among authors: krebsova a. Hum Genet. 1997 May;99(5):565-72. doi: 10.1007/s004390050407. Hum Genet. 1997. PMID: 9150719

3

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

Dörk T, Macek M Jr, Mekus F, Tümmler B, Tzountzouris J, Casals T, Krebsová A, Koudová M, Sakmaryová I, Macek M Sr, Vávrová V, Zemková D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zékanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S. Dörk T, et al. Among authors: krebsova a. Hum Genet. 2000 Mar;106(3):259-68. doi: 10.1007/s004390000246. Hum Genet. 2000. PMID: 10798353

4

[Cystic fibrosis--a disease of adolescents and adults?].

Vávrová V, Zemková D, Bartosová J, Zapletal A, Smolíková L, Krebsová A, Koudová M, Macek M Jr. Vávrová V, et al. Among authors: krebsova a. Cas Lek Cesk. 1999 Nov 1;138(21):654-9. Cas Lek Cesk. 1999. PMID: 10746022 Czech.

5

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.

Riess O, Schöls L, Bottger H, Nolte D, Vieira-Saecker AM, Schimming C, Kreuz F, Macek M Jr, Krebsová A, Macek M Sen, Klockgether T, Zühlke C, Laccone FA. Riess O, et al. Among authors: krebsova a. Hum Mol Genet. 1997 Aug;6(8):1289-93. doi: 10.1093/hmg/6.8.1289. Hum Mol Genet. 1997. PMID: 9259275

6

[Chromosome Y microdeletions in Czech men with severe reproductive disorders].

Machatková M, Krebsová A, Smetanová I, Matĕjcková M, Vilímová S, Sobek A, Macek M Sr. Machatková M, et al. Among authors: krebsova a. Cas Lek Cesk. 2003;142(11):670-5. Cas Lek Cesk. 2003. PMID: 14689827 Slovak.

7

Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity.

Krebsová A, Küster W, Lestringant GG, Schulze B, Hinz B, Frossard PM, Reis A, Hennies HC. Krebsová A, et al. Am J Hum Genet. 2001 Jul;69(1):216-22. doi: 10.1086/321284. Epub 2001 Jun 7. Am J Hum Genet. 2001. PMID: 11398099 Free PMC article.

8

Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.

de Brouwer AP, Kunst HP, Krebsova A, van Asseldonk K, Reis A, Snoeckx RL, Van Camp G, Cremers CW, Cremers FP, Kremer H. de Brouwer AP, et al. Among authors: krebsova a. Am J Med Genet A. 2005 Aug 15;137(1):41-6. doi: 10.1002/ajmg.a.30844. Am J Med Genet A. 2005. PMID: 16007628

9

Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: redefining a clinical entity.

Horn D, Krebsová A, Kunze J, Reis A. Horn D, et al. Among authors: krebsova a. Am J Med Genet. 2000 Jun 5;92(4):285-92. Am J Med Genet. 2000. PMID: 10842298

10

[Treatment of infertility in non-obstructive azoospermia using the TESE (testicular sperm extraction) method--clinical study].

Sobek A, Hrbková K, Mucha Z, Tesarová M, Priesnitz J, Zát'ura F, Scheinar J, Macek M, Krebsová A, Macek M Jr, Bártek J. Sobek A, et al. Among authors: krebsova a. Ceska Gynekol. 1998 Aug;63(4):287-91. Ceska Gynekol. 1998. PMID: 9750403 Czech.

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