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Kathelijn Keymolen

Showing results (1-10 of 61) with videos related to

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Handbook of Clinical Neurology|July 21, 2019
Fetal and neonatal neurogeneticsAnna C Jansen, Kathelijn Keymolen
European Journal of Human Genetics : EJHG|November 11, 2011
Preimplantation genetic diagnosis in female and male carriers of reciprocal translocations: clinical outcome until delivery of 312 cyclesKathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
American Journal of Medical Genetics. Part A|December 17, 2009
Floating-Harbor syndrome associated with middle ear abnormalitiesJan-Jaap Hendrickx, Kathelijn Keymolen, Brigitte Desprechins, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Pregnancy outcome in carriers of Robertsonian translocationsKathelijn Keymolen, Kim Van Berkel, Anniek Vorsselmans, et al.
Journal of the Neurological Sciences|July 15, 2011
A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperatureVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Human Molecular Genetics|June 5, 2003
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasiaElisabeth Sock, Roberta A Pagon, Kathelijn Keymolen, et al.
Neuromuscular Disorders : NMD|June 14, 2011
Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutationVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Reproductive Biomedicine Online|December 21, 2021
Analysis of parental contribution for aneuploidy detection (APCAD): a novel method to detect aneuploidy and mosaicism in preimplantation embryosPieter Verdyck, Veerle Berckmoes, Sven Van Laere, et al.
Genes|February 26, 2025
APCAD Part 2: A Novel Method for Detection of Meiotic Aneuploidy in Preimplantation EmbryosPieter Verdyck, Veerle Berckmoes, Elia Fernandez Gallardo, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Handbook of Clinical Neurology|July 21, 2019
Fetal and neonatal neurogeneticsAnna C Jansen, Kathelijn Keymolen
European Journal of Human Genetics : EJHG|November 11, 2011
Preimplantation genetic diagnosis in female and male carriers of reciprocal translocations: clinical outcome until delivery of 312 cyclesKathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
American Journal of Medical Genetics. Part A|December 17, 2009
Floating-Harbor syndrome associated with middle ear abnormalitiesJan-Jaap Hendrickx, Kathelijn Keymolen, Brigitte Desprechins, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Pregnancy outcome in carriers of Robertsonian translocationsKathelijn Keymolen, Kim Van Berkel, Anniek Vorsselmans, et al.
Journal of the Neurological Sciences|July 15, 2011
A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperatureVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Human Molecular Genetics|June 5, 2003
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasiaElisabeth Sock, Roberta A Pagon, Kathelijn Keymolen, et al.
Neuromuscular Disorders : NMD|June 14, 2011
Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutationVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Reproductive Biomedicine Online|December 21, 2021
Analysis of parental contribution for aneuploidy detection (APCAD): a novel method to detect aneuploidy and mosaicism in preimplantation embryosPieter Verdyck, Veerle Berckmoes, Sven Van Laere, et al.
Genes|February 26, 2025
APCAD Part 2: A Novel Method for Detection of Meiotic Aneuploidy in Preimplantation EmbryosPieter Verdyck, Veerle Berckmoes, Elia Fernandez Gallardo, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Pageof 7