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M Alders

Showing results (31-40 of 44) with videos related to

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Forensic Science International|April 10, 2017
Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A geneT Jenewein, B M Beckmann, S Rose, et al.
Genomics|June 1, 1997
Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2M A Nesbit, M D Hodges, L Campbell, et al.
Clinical Epigenetics|March 23, 2019
Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnosticsI M Krzyzewska, M Alders, S M Maas, et al.
Medical and Pediatric Oncology|November 1, 1996
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumorsM Mannens, M Alders, B Redeker, et al.
European Journal of Medical Genetics|May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris SyndromeSarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsJ M Hoovers, L M Kalikin, L A Johnson, et al.
Human Reproduction (Oxford, England)|November 10, 2021
Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexesM J Wyrwoll, E S van Walree, G Hamer, et al.
Journal of Medical Genetics|August 6, 2010
Epigenotype-phenotype correlations in Silver-Russell syndromeE L Wakeling, S Abu Amero, M Alders, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996T B Shows, M Alders, S Bennett, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Forensic Science International|April 10, 2017
Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A geneT Jenewein, B M Beckmann, S Rose, et al.
Genomics|June 1, 1997
Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2M A Nesbit, M D Hodges, L Campbell, et al.
Clinical Epigenetics|March 23, 2019
Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnosticsI M Krzyzewska, M Alders, S M Maas, et al.
Medical and Pediatric Oncology|November 1, 1996
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumorsM Mannens, M Alders, B Redeker, et al.
European Journal of Medical Genetics|May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris SyndromeSarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsJ M Hoovers, L M Kalikin, L A Johnson, et al.
Human Reproduction (Oxford, England)|November 10, 2021
Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexesM J Wyrwoll, E S van Walree, G Hamer, et al.
Journal of Medical Genetics|August 6, 2010
Epigenotype-phenotype correlations in Silver-Russell syndromeE L Wakeling, S Abu Amero, M Alders, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996T B Shows, M Alders, S Bennett, et al.
Pageof 5