Mayerova A - Search Results

1

Dopamine D3 receptor gene: organization, transcript variants, and polymorphism associated with schizophrenia.

Griffon N, Crocq MA, Pilon C, Martres MP, Mayerova A, Uyanik G, Burgert E, Duval F, Macher JP, Javoy-Agid F, Tamminga CA, Schwartz JC, Sokoloff P. Griffon N, et al. Among authors: mayerova a. Am J Med Genet. 1996 Feb 16;67(1):63-70. doi: 10.1002/(SICI)1096-8628(19960216)67:1<63::AID-AJMG11>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8678117

2

Association between schizophrenia and homozygosity at the dopamine D3 receptor gene.

Crocq MA, Mant R, Asherson P, Williams J, Hode Y, Mayerova A, Collier D, Lannfelt L, Sokoloff P, Schwartz JC, et al. Crocq MA, et al. Among authors: mayerova a. J Med Genet. 1992 Dec;29(12):858-60. doi: 10.1136/jmg.29.12.858. J Med Genet. 1992. PMID: 1362221 Free PMC article.

3

BalI and MspI polymorphisms of the dopamine D3 receptor gene in African Blacks and Caucasians.

Crocq MA, Buguet A, Bisser S, Burgert E, Stanghellini A, Uyanik G, Dumas M, Macher JP, Mayerova A. Crocq MA, et al. Among authors: mayerova a. Hum Hered. 1996 Jan-Feb;46(1):58-60. doi: 10.1159/000154327. Hum Hered. 1996. PMID: 8825465

4

Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.

Morris-Rosendahl DJ, Burgert E, Uyanik G, Mayerova A, Duval F, Macher JP, Crocq MA. Morris-Rosendahl DJ, et al. Among authors: mayerova a. Am J Med Genet. 1997 May 31;74(3):324-30. doi: 10.1002/(sici)1096-8628(19970531)74:3<324::aid-ajmg15>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9184318

5

Aldosterone deficiency II (CMO II deficiency) is not the result of a mutation of an MspI restriction site within the CYP11B gene.

Mayerovà A, Zieger B, Brandis M, von Petrykowski W, Wolff G. Mayerovà A, et al. Hum Genet. 1991 May;87(1):97-8. doi: 10.1007/BF01213103. Hum Genet. 1991. PMID: 1709913

6

Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

Wolff G, Mayerová A, Wienker TF, Atalianis P, Ioannou P, Warburg M. Wolff G, et al. Among authors: mayerova a. J Med Genet. 1992 Nov;29(11):816-9. doi: 10.1136/jmg.29.11.816. J Med Genet. 1992. PMID: 1453434 Free PMC article.

7

Haptoglobin types in gypsies from Slovakia (Czechoslovakia).

Gáliková J, Vilímová M, Ferák V, Mayerová A. Gáliková J, et al. Among authors: mayerova a. Hum Hered. 1969;19(5):480-5. doi: 10.1159/000152256. Hum Hered. 1969. PMID: 5365886 No abstract available.

8

[Genetic counseling in prenatal diagnosis of cystic fibrosis].

Wolff G, Mayerová A. Wolff G, et al. Among authors: mayerova a. Monatsschr Kinderheilkd. 1991 May;139(5):275-81. Monatsschr Kinderheilkd. 1991. PMID: 1870597 Review. German.

9

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.

Dörk T, Dworniczak B, Aulehla-Scholz C, Wieczorek D, Böhm I, Mayerova A, Seydewitz HH, Nieschlag E, Meschede D, Horst J, Pander HJ, Sperling H, Ratjen F, Passarge E, Schmidtke J, Stuhrmann M. Dörk T, et al. Among authors: mayerova a. Hum Genet. 1997 Sep;100(3-4):365-77. doi: 10.1007/s004390050518. Hum Genet. 1997. PMID: 9272157

10

Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal life.

Kuhnle U, Böhm N, Wolff G, Mayerová A, Dörr HG, Bidlingmaier F, Knorr D. Kuhnle U, et al. Among authors: mayerova a. J Clin Endocrinol Metab. 1984 Mar;58(3):574-7. doi: 10.1210/jcem-58-3-574. J Clin Endocrinol Metab. 1984. PMID: 6607266

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

72 results

Search Page