Kosztolányi G - Search Results

1

Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population.

Gyürüs P, Molnár J, Melegh B, Tóth G, Morava E, Kosztolányi G, Méhes K. Gyürüs P, et al. Among authors: kosztolanyi g. Am J Med Genet. 1999 Nov 26;87(3):245-50. doi: 10.1002/(sici)1096-8628(19991126)87:3<245::aid-ajmg9>3.3.co;2-5. Am J Med Genet. 1999. PMID: 10564878

2

Premature centromere division of a translocation-carrier autosome.

Méhes K, Kosztolányi G. Méhes K, et al. Among authors: kosztolanyi g. Hum Genet. 1990 Aug;85(3):379-80. doi: 10.1007/BF00206765. Hum Genet. 1990. PMID: 2203674

3

Morphologic variants in parents of children with malformation syndromes: are they indicators of somatic mosaicism?

Méhes K, Kosztolányi G. Méhes K, et al. Among authors: kosztolanyi g. Clin Genet. 1990 Aug;38(2):114-6. doi: 10.1111/j.1399-0004.1990.tb03557.x. Clin Genet. 1990. PMID: 2208761

4

Cohen syndrome: a connective tissue disorder?

Méhes K, Kosztolányi G, Kardos M, Horváth M. Méhes K, et al. Among authors: kosztolanyi g. Am J Med Genet. 1988 Sep;31(1):131-3. doi: 10.1002/ajmg.1320310115. Am J Med Genet. 1988. PMID: 3223494

5

Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation.

Kosztolányi G, Weisenbach J, Méhes K. Kosztolányi G, et al. Am J Med Genet. 1995 Sep 11;58(3):213-6. doi: 10.1002/ajmg.1320580303. Am J Med Genet. 1995. PMID: 8533819

6

X-linked mental retardation syndrome: three brothers with the Brooks-Wisniewski-Brown syndrome.

Morava E, Storcz J, Kosztolányi G. Morava E, et al. Among authors: kosztolanyi g. Am J Med Genet. 1996 Jul 12;64(1):59-62. doi: 10.1002/(SICI)1096-8628(19960712)64:1<59::AID-AJMG8>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826449

7

Isodicentric Y chromosome in an Ullrich-Turner patient without virilization.

Morava E, Hermann R, Czakó M, Soltész G, Kosztolányi G. Morava E, et al. Among authors: kosztolanyi g. Am J Med Genet. 2000 Mar 13;91(2):99-101. doi: 10.1002/(sici)1096-8628(20000313)91:2<99::aid-ajmg3>3.0.co;2-c. Am J Med Genet. 2000. PMID: 10748405

8

Distribution of Q188R and N314D mutations in the Hungarian galactosemic population.

Horváth A, Gyurus P, Kis A, László A, Schuler A, Kosztolányi G, Melegh B. Horváth A, et al. Among authors: kosztolanyi g. Hum Mutat. 2000 Jul;16(1):91. doi: 10.1002/1098-1004(200007)16:1<91::AID-HUMU21>3.0.CO;2-D. Hum Mutat. 2000. PMID: 10874317

9

Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children.

Morava E, Czakó M, Melegh B, Kosztolányi G. Morava E, et al. Among authors: kosztolanyi g. Clin Genet. 2000 Nov;58(5):403-5. doi: 10.1034/j.1399-0004.2000.580512.x. Clin Genet. 2000. PMID: 11140842

10

Association of nonsyndromic Wilms tumor with premature centromere division (PCD).

Méhes K, Kajtár P, Kosztolányi G. Méhes K, et al. Among authors: kosztolanyi g. Am J Med Genet. 2002 Oct 1;112(2):215-6. doi: 10.1002/ajmg.10661. Am J Med Genet. 2002. PMID: 12244559

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