New KIT mutations in patients with piebaldism
Murakami, Tomoko, Fukai, Kazuyoshi, Oiso, Naoki, Hosomi, Naoko, Kato, Atsushi, Garganta, Cheryl, Barnicoat, Angela, Poppelaars, Francis, Aquaron, Robert, Paller, Amy S, Ishii, Masamitsu
Published in Journal of dermatological science (01.06.2004)
Published in Journal of dermatological science (01.06.2004)
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Journal Article
Current practice and future interest of GPs and prospective parents in pre-conception care in The Netherlands
Poppelaars, Francis AM, Cornel, Martina C, ten Kate, Leo P
Published in Family practice (01.06.2004)
Published in Family practice (01.06.2004)
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Journal Article
Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria
Henneman, Lidewij, Poppelaars, Francis A.M., ten Kate, Leo P.
Published in Genetics in medicine (01.07.2002)
Published in Genetics in medicine (01.07.2002)
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Journal Article
Attitudes of Potential Providers Towards Preconceptional Cystic Fibrosis Carrier Screening
Poppelaars, Francis A. M., Adèr, Herman J., Cornel, Martina C., Henneman, Lidewij, Hermens, Rosella P. M. G., Wal, Gerrit, Kate, Leo P. ten
Published in Journal of genetic counseling (01.02.2004)
Published in Journal of genetic counseling (01.02.2004)
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Journal Article
How Should Preconceptional Cystic Fibrosis Carrier Screening Be Provided? Opinions of Potential Providers and the Target Population
Poppelaars, Francis A.M., Henneman, Lidewij, Adèr, Herman J., Cornel, Martina C., Hermens, Rosella P.M.G., van der Wal, Gerrit, ten Kate, Leo P.
Published in Community genetics (2003)
Published in Community genetics (2003)
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Journal Article
Expanding phenotype of XNP mutations: mild to moderate mental retardation
Yntema, Helger G, Poppelaars, Francis A, Derksen, Esther, Oudakker, Astrid R, van Roosmalen, Tanja, Jacobs, Anja, Obbema, Hanneke, Brunner, Han G, Hamel, Ben C J, van Bokhoven, Hans
Published in American journal of medical genetics (01.07.2002)
Published in American journal of medical genetics (01.07.2002)
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Journal Article
Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3
Kleefstra, Tjitske, Yntema, Helger G, Oudakker, Astrid R, de Vries, Bert B A, van Bokhoven, Hans, Hamel, Ben C J, Poppelaars, Francis A, Ausems, Margreet G E M
Published in American journal of medical genetics (15.07.2002)
Published in American journal of medical genetics (15.07.2002)
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Journal Article
Preconceptional cystic fibrosis carrier screening: attitudes and intentions of the target population
Poppelaars, Francis A M, Henneman, Lidewij, Adèr, Herman J, Cornel, Martina C, Hermens, Rosella P M G, van der Wal, Gerrit, ten Kate, Leo P
Published in Genetic testing (01.06.2004)
Published in Genetic testing (01.06.2004)
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Journal Article
Preconception cystic fibrosis carrier screening: costs and consequences
Weijers-Poppelaars, Francis A M, Wildhagen, Mark F, Henneman, Lidewij, Cornel, Martina C, Kate, Leo P Ten
Published in Genetic testing (01.06.2005)
Published in Genetic testing (01.06.2005)
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Journal Article
A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation
Yntema, Helger G., van den Helm, Bellinda, Kissing, Johan, van Duijnhoven, Gerard, Poppelaars, Francis, Chelly, Jamel, Moraine, Claude, Fryns, Jean-Pierre, Hamel, Ben C.J., Heilbronner, Helmut, Pander, Hans-Jürgen, Brunner, Han G., Ropers, Hans-Hilger, Cremers, Frans P.M., van Bokhoven, Hans
Published in Genomics (San Diego, Calif.) (15.12.1999)
Published in Genomics (San Diego, Calif.) (15.12.1999)
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