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Journal of Reproductive and Infant Psychology
|
October 22, 2025
The influence of termination of pregnancy for foetal abnormality on subsequent reproductive decision-making
Ileen Slegers, Kathelijn Keymolen, Chris Winter, et al.
Minerva Pediatrica
|
September 9, 2016
Can clinical characteristics be criteria to perform chromosomal microarray analysis in children and adolescents with autism spectrum disorders?
Melissa Sys, Ann van den Bogaert, Bram Roosens, et al.
Human Reproduction (Oxford, England)
|
June 5, 2009
A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosis
Kathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
Human Reproduction (Oxford, England)
|
September 28, 2002
Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parameters
Maryse Bonduelle, Elvire Van Assche, Hubert Joris, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 19, 2016
Gastric emptying and gastro-oesophageal reflux in children with cystic fibrosis
Bruno Hauser, Jean De Schepper, Anne Malfroot, et al.
Reproduction (Cambridge, England)
|
October 28, 2020
PREIMPLANTATION GENETIC TESTING: Clinical experience of preimplantation genetic testing
Martine De Rycke, Veerle Berckmoes, Anick De Vos, et al.
European Journal of Human Genetics : EJHG
|
May 12, 2023
Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for congenital malformations
Ileen Slegers, Kathelijn Keymolen, Kim Van Berkel, et al.
Acta Neurologica Belgica
|
August 4, 2025
"Phenotypic and genotypic insights, counseling strategies, and follow-up in 24 individuals with filamin a deficiency: findings from a retrospective cohort study"
Ellen Rijckmans, Lars De Strooper, Kathelijn Keymolen, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2007
Clinical outcome of preimplantation genetic diagnosis for cystic fibrosis: the Brussels' experience
Kathelijn Keymolen, Veerle Goossens, Martine De Rycke, et al.
European Journal of Pediatrics
|
September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndrome
Sara Seneca, Domique Fagnart, Kathelijn Keymolen, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 61) with videos related to
Sort By:
Page
of 7
Journal of Reproductive and Infant Psychology
|
October 22, 2025
The influence of termination of pregnancy for foetal abnormality on subsequent reproductive decision-making
Ileen Slegers, Kathelijn Keymolen, Chris Winter, et al.
Minerva Pediatrica
|
September 9, 2016
Can clinical characteristics be criteria to perform chromosomal microarray analysis in children and adolescents with autism spectrum disorders?
Melissa Sys, Ann van den Bogaert, Bram Roosens, et al.
Human Reproduction (Oxford, England)
|
June 5, 2009
A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosis
Kathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
Human Reproduction (Oxford, England)
|
September 28, 2002
Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parameters
Maryse Bonduelle, Elvire Van Assche, Hubert Joris, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 19, 2016
Gastric emptying and gastro-oesophageal reflux in children with cystic fibrosis
Bruno Hauser, Jean De Schepper, Anne Malfroot, et al.
Reproduction (Cambridge, England)
|
October 28, 2020
PREIMPLANTATION GENETIC TESTING: Clinical experience of preimplantation genetic testing
Martine De Rycke, Veerle Berckmoes, Anick De Vos, et al.
European Journal of Human Genetics : EJHG
|
May 12, 2023
Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for congenital malformations
Ileen Slegers, Kathelijn Keymolen, Kim Van Berkel, et al.
Acta Neurologica Belgica
|
August 4, 2025
"Phenotypic and genotypic insights, counseling strategies, and follow-up in 24 individuals with filamin a deficiency: findings from a retrospective cohort study"
Ellen Rijckmans, Lars De Strooper, Kathelijn Keymolen, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2007
Clinical outcome of preimplantation genetic diagnosis for cystic fibrosis: the Brussels' experience
Kathelijn Keymolen, Veerle Goossens, Martine De Rycke, et al.
European Journal of Pediatrics
|
September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndrome
Sara Seneca, Domique Fagnart, Kathelijn Keymolen, et al.
Page
of 7