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D J Halley

Showing results (11-20 of 96) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|November 24, 1990
[Carrier detection in relatives of patients with cystic fibrosis and their partners]L P ten Kate, H Scheffer, D J Halley, et al.
Acta Neurologica Scandinavica. Supplementum|January 1, 1992
In search for genes predisposing to epilepsy: motives and methodsD Lindhout, T Sander, D J Halley, et al.
Journal of Intellectual Disability Research : JIDR|February 1, 1994
The fragile-X syndrome: a growing gene causing familial intellectual disabilityL B De Vries, D J Halley, B A Oostra, et al.
Journal of Medical Genetics|July 25, 1998
The fragile X syndromeB B de Vries, D J Halley, B A Oostra, et al.
Biochemical and Biophysical Research Communications|June 29, 1978
The distribution of hydrolytic enzyme activities in human fibroblast cultures and their intercellular transferD J Halley, H A de Wit-Verbeek, A J Reuser, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 29, 1998
[Prader-Willi syndrome in a young infant]W W Hack, R ten Houten, E J Breslau-Suderius, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1989
Prenatal diagnosis and genetic counseling of cystic fibrosisM F Niermeijer, D J Halley, W J Kleijer, et al.
American Journal of Medical Genetics|August 17, 1999
Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formationC van den Berg, L Pijpers, D J Halley, et al.
Journal of Medical Genetics|October 3, 1999
Angelman syndrome: AS phenotype correlated with specific EEG pattern may result in a high detection rate of mutations in the UBE3A geneA M van den Ouweland, P L Bakker, D J Halley, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 5, 2002
[From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy]A L Boehmer, A O Brinkmann, M F Niermeijer, et al.
Pageof 10

Showing results (11-20 of 96) with videos related to

Sort By:
Pageof 10
Nederlands Tijdschrift Voor Geneeskunde|November 24, 1990
[Carrier detection in relatives of patients with cystic fibrosis and their partners]L P ten Kate, H Scheffer, D J Halley, et al.
Acta Neurologica Scandinavica. Supplementum|January 1, 1992
In search for genes predisposing to epilepsy: motives and methodsD Lindhout, T Sander, D J Halley, et al.
Journal of Intellectual Disability Research : JIDR|February 1, 1994
The fragile-X syndrome: a growing gene causing familial intellectual disabilityL B De Vries, D J Halley, B A Oostra, et al.
Journal of Medical Genetics|July 25, 1998
The fragile X syndromeB B de Vries, D J Halley, B A Oostra, et al.
Biochemical and Biophysical Research Communications|June 29, 1978
The distribution of hydrolytic enzyme activities in human fibroblast cultures and their intercellular transferD J Halley, H A de Wit-Verbeek, A J Reuser, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 29, 1998
[Prader-Willi syndrome in a young infant]W W Hack, R ten Houten, E J Breslau-Suderius, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1989
Prenatal diagnosis and genetic counseling of cystic fibrosisM F Niermeijer, D J Halley, W J Kleijer, et al.
American Journal of Medical Genetics|August 17, 1999
Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formationC van den Berg, L Pijpers, D J Halley, et al.
Journal of Medical Genetics|October 3, 1999
Angelman syndrome: AS phenotype correlated with specific EEG pattern may result in a high detection rate of mutations in the UBE3A geneA M van den Ouweland, P L Bakker, D J Halley, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 5, 2002
[From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy]A L Boehmer, A O Brinkmann, M F Niermeijer, et al.
Pageof 10