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J Gécz

Showing results (1-10 of 29) with videos related to

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Journal of Medical Genetics|October 4, 2000
FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutationsJ Gécz
Nucleic Acids Research|October 25, 1991
PCR amplification of large VNTR alleles of D17S5 (YNZ22) locusJ Gécz
Bratislavske Lekarske Listy|June 1, 1993
[DNA diagnosis of hemophilia A in a family without an affected proband]J Gécz
Genome Research|February 15, 2000
Genes for cognitive function: developments on the XJ Gécz, J Mulley
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1991
Frequency and distribution of deletions in dystrophin gene in Duchenne muscular dystrophy patients from an east-European Slavonic populationL Kádasi, J Gécz, L Saksová
Bratislavske Lekarske Listy|September 1, 1992
[Identification of a de novo mutation in a factor FVIII:C gene in a family requesting prenatal diagnosis of hemophilia A]J Gécz, L Saksová, L Kádasi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2003
Brain cysts associated with mutation in the Aristaless related homeobox gene, ARXP Strømme, S J Bakke, A Dahl, et al.
Clinical Genetics|June 18, 2004
Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARXM W Partington, G Turner, J Boyle, et al.
Bratislavske Lekarske Listy|May 1, 1993
[Molecular genetic analysis of deletions in the Duchenne and Becker types of progressive muscular dystrophy]L Kádasi, J Gécz, L Saksová, et al.
Cytogenetic and Genome Research|August 6, 2003
Evolution of the human X--a smart and sexy chromosome that controls speciation and developmentJ A M Graves, J Gécz, H Hameister
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|October 4, 2000
FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutationsJ Gécz
Nucleic Acids Research|October 25, 1991
PCR amplification of large VNTR alleles of D17S5 (YNZ22) locusJ Gécz
Bratislavske Lekarske Listy|June 1, 1993
[DNA diagnosis of hemophilia A in a family without an affected proband]J Gécz
Genome Research|February 15, 2000
Genes for cognitive function: developments on the XJ Gécz, J Mulley
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1991
Frequency and distribution of deletions in dystrophin gene in Duchenne muscular dystrophy patients from an east-European Slavonic populationL Kádasi, J Gécz, L Saksová
Bratislavske Lekarske Listy|September 1, 1992
[Identification of a de novo mutation in a factor FVIII:C gene in a family requesting prenatal diagnosis of hemophilia A]J Gécz, L Saksová, L Kádasi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2003
Brain cysts associated with mutation in the Aristaless related homeobox gene, ARXP Strømme, S J Bakke, A Dahl, et al.
Clinical Genetics|June 18, 2004
Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARXM W Partington, G Turner, J Boyle, et al.
Bratislavske Lekarske Listy|May 1, 1993
[Molecular genetic analysis of deletions in the Duchenne and Becker types of progressive muscular dystrophy]L Kádasi, J Gécz, L Saksová, et al.
Cytogenetic and Genome Research|August 6, 2003
Evolution of the human X--a smart and sexy chromosome that controls speciation and developmentJ A M Graves, J Gécz, H Hameister
Pageof 3