Cancer genetics and insurance.

Yazar: Niermeijer, M F
Baskı/Yayın Bilgisi 1999

The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis.

Yazar: De Vries, B B, Niermeijer, M F
Baskı/Yayın Bilgisi 1994

Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations.

Yazar: Schonberg, S, Niermeijer, M F, Bootsma, D, Henderson, E, German, J
Baskı/Yayın Bilgisi 1984

A Decade of Genetic Counseling in Frontotemporal Dementia Affected Families: Few Counseling Requests and much Familial Opposition to Testing

Yazar: Riedijk, S. R., Niermeijer, M. F. N., Dooijes, D., Tibben, A.
Baskı/Yayın Bilgisi 2009

The fragile X syndrome.

Yazar: de Vries, B B, Halley, D J, Oostra, B A, Niermeijer, M F
Baskı/Yayın Bilgisi 1998

Predicting adaptation to presymptomatic DNA testing for late onset disorders: who will experience distress? Rotterdam Leiden Genetics Workgroup.

Yazar: DudokdeWit, A C, Tibben, A, Duivenvoorden, H J, Niermeijer, M F, Passchier, J
Baskı/Yayın Bilgisi 1998

Prenatal diagnosis of genetic disorders.

Yazar: Niermeijer, M F, Sachs, E S, Jahodova, M, Tichelaar-Klepper, C, Kleijer, W J, Galjaard, H
Baskı/Yayın Bilgisi 1976

Analysis of problems in making the reproductive decision after genetic counselling.

Yazar: Frets, P G, Duivenvoorden, H J, Verhage, F, Peters-Romeyn, B M, Niermeijer, M F
Baskı/Yayın Bilgisi 1991

Germ-line and somatic mosaicism in the androgen insensitivity syndrome: implications for genetic counseling.

Yazar: Boehmer, A L, Brinkmann, A O, Niermeijer, M F, Bakker, L, Halley, D J, Drop, S L
Baskı/Yayın Bilgisi 1997

Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.

Yazar: Van Hemel, J O, Schaap, C, Van Opstal, D, Mulder, M P, Niermeijer, M F, Meijers, J H
Baskı/Yayın Bilgisi 1995

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

Yazar: van der Steenstraten, I. M., Tibben, A., Roos, R. A., van de Kamp, J. J., Niermeijer, M. F.
Baskı/Yayın Bilgisi 1994

Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease.

Yazar: Tibben, A, Stevens, M, de Wert, G M, Niermeijer, M F, van Duijn, C M, van Swieten, J C
Baskı/Yayın Bilgisi 1997

DNA testing for fragile X syndrome: implications for parents and family.

Yazar: van Rijn, M A, de Vries, B B, Tibben, A, van den Ouweland, A M, Halley, D J, Niermeijer, M F
Baskı/Yayın Bilgisi 1997

Minor disease features in neurofibromatosis type 1 (NF1) and their possible value in diagnosis of NF1 in children < or = 6 years and clinically suspected of having NF1. Neurofibrom...

Yazar: Cnossen, M H, Moons, K G, Garssen, M P, Pasmans, N M, de Goede-Bolder, A, Niermeijer, M F, Grobbee, D E
Baskı/Yayın Bilgisi 1998

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup.

Yazar: DudokdeWit, A C, Tibben, A, Duivenvoorden, H J, Frets, P G, Zoeteweij, M W, Losekoot, M, van Haeringen, A, Niermeijer, M F, Passchier, J
Baskı/Yayın Bilgisi 1997

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

Yazar: Heutink, P, van de Wetering, B J, Breedveld, G J, Weber, J, Sandkuyl, L A, Devor, E J, Heiberg, A, Niermeijer, M F, Oostra, B A
Baskı/Yayın Bilgisi 1990

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

Yazar: de Vries, B B, Fryns, J P, Butler, M G, Canziani, F, Wesby-van Swaay, E, van Hemel, J O, Oostra, B A, Halley, D J, Niermeijer, M F
Baskı/Yayın Bilgisi 1993

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Yazar: Meijers-Heijboer, E J, Sandkuijl, L A, Brunner, H G, Smeets, H J, Hoogeboom, A J, Deelen, W H, van Hemel, J O, Nelen, M R, Smeets, D F, Niermeijer, M F
Baskı/Yayın Bilgisi 1992

Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.

Yazar: de Vries, B B, Jansen, C C, Duits, A A, Verheij, C, Willemsen, R, van Hemel, J O, van den Ouweland, A M, Niermeijer, M F, Oostra, B A, Halley, D J
Baskı/Yayın Bilgisi 1996

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Yazar: Rizzu, P, Van Swieten, J C, Joosse, M, Hasegawa, M, Stevens, M, Tibben, A, Niermeijer, M F, Hillebrand, M, Ravid, R, Oostra, B A, Goedert, M, van Duijn, C M, Heutink, P
Baskı/Yayın Bilgisi 1999