Méhes K - Search Results

1

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.

Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie IW, Ilyina H, Méhes K, Hamel BC, Otten BJ, Hergersberg M, et al. Kotzot D, et al. Among authors: mehes k. Hum Mol Genet. 1995 Apr;4(4):583-7. doi: 10.1093/hmg/4.4.583. Hum Mol Genet. 1995. PMID: 7633407 Free article.

2

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation.

Kotzot D, Lurie IW, Méhes K, Werder E, Schinzel A. Kotzot D, et al. Among authors: mehes k. Clin Genet. 2000 Sep;58(3):177-80. doi: 10.1034/j.1399-0004.2000.580304.x. Clin Genet. 2000. PMID: 11076039

3

Parental centromere separation sequence and aneuploidy in the offspring.

Bajnóczky K, Méhes K. Bajnóczky K, et al. Among authors: mehes k. Hum Genet. 1988 Mar;78(3):286-8. doi: 10.1007/BF00291679. Hum Genet. 1988. PMID: 2964398

4

A possible mosaic form of delayed centromere separation and aneuploidy.

Méhes K, Kosztolányi G. Méhes K, et al. Hum Genet. 1992 Feb;88(4):477-8. doi: 10.1007/BF00215686. Hum Genet. 1992. PMID: 1740325

5

Inherited ring chromosomes: an analysis of published cases.

Kosztolányi G, Méhes K, Hook EB. Kosztolányi G, et al. Among authors: mehes k. Hum Genet. 1991 Jul;87(3):320-4. doi: 10.1007/BF00200912. Hum Genet. 1991. PMID: 1864607 Review.

6

Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B.

Hanks S, Coleman K, Reid S, Plaja A, Firth H, Fitzpatrick D, Kidd A, Méhes K, Nash R, Robin N, Shannon N, Tolmie J, Swansbury J, Irrthum A, Douglas J, Rahman N. Hanks S, et al. Among authors: mehes k. Nat Genet. 2004 Nov;36(11):1159-61. doi: 10.1038/ng1449. Epub 2004 Oct 10. Nat Genet. 2004. PMID: 15475955 Free article.

7

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

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

8

Premature centromere division of a translocation-carrier autosome.

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

9

Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion.

Bene J, Nádasi E, Kosztolányi G, Méhes K, Melegh B. Bene J, et al. Among authors: mehes k. Eur J Hum Genet. 2003 May;11(5):375-9. doi: 10.1038/sj.ejhg.5200975. Eur J Hum Genet. 2003. PMID: 12734542

10

Unusually early dividing chromosomes 13-15 in a child with retinoblastoma and 13q deletion.

Méhes K, Bajnóczky K. Méhes K, et al. Hum Genet. 1982;61(1):78. doi: 10.1007/BF00291342. Hum Genet. 1982. PMID: 7129434 No abstract available.

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