Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Maat

Showing results (21-30 of 52) with videos related to

Pageof 6
Sort By:
Prenatal Diagnosis|June 9, 1999
Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987-1997)A Maat-Kievit, M Vegter-van der Vlis, M Zoeteweij, et al.
Journal of Clinical and Experimental Neuropsychology|January 29, 2000
Memory and learning are not impaired in presymptomatic individuals with an increased risk of Huntington's diseaseG M de Boo, A A Tibben, J A Hermans, et al.
Archives of Neurology|November 18, 1997
Early cognitive and motor symptoms in identified carriers of the gene for Huntington diseaseG M de Boo, A Tibben, J B Lanser, et al.
Prenatal Diagnosis|May 1, 1993
A large retinoblastoma detected in a fetus at 21 weeks of gestationJ A Maat-Kievit, D Oepkes, N G Hartwig, et al.
Journal of Medical Genetics|April 3, 2001
New problems in testing for Huntington's disease: the issue of intermediate and reduced penetrance allelesA Maat-Kievit, M Losekoot, H Van Den Boer-Van Den Berg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 23, 2000
Family history and DNA analysis in patients with suspected Huntington's diseaseS Siesling, M Vegter-van de Vlis, M Losekoot, et al.
Journal of Medical Genetics|November 3, 2004
A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15G J Breedveld, B van Wetten, G D te Raa, et al.
Journal of Medical Genetics|April 16, 1999
Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacitiesA T Helderman-van den Enden, P D Maaswinkel-Mooij, E Hoogendoorn, et al.
Journal of Medical Genetics|October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeB Horsthemke, A Maat-Kievit, E Sleegers, et al.
American Journal of Medical Genetics|January 23, 2002
Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington diseaseA Maat-Kievit, P Helderman-van den Enden, M Losekoot, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|June 9, 1999
Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987-1997)A Maat-Kievit, M Vegter-van der Vlis, M Zoeteweij, et al.
Journal of Clinical and Experimental Neuropsychology|January 29, 2000
Memory and learning are not impaired in presymptomatic individuals with an increased risk of Huntington's diseaseG M de Boo, A A Tibben, J A Hermans, et al.
Archives of Neurology|November 18, 1997
Early cognitive and motor symptoms in identified carriers of the gene for Huntington diseaseG M de Boo, A Tibben, J B Lanser, et al.
Prenatal Diagnosis|May 1, 1993
A large retinoblastoma detected in a fetus at 21 weeks of gestationJ A Maat-Kievit, D Oepkes, N G Hartwig, et al.
Journal of Medical Genetics|April 3, 2001
New problems in testing for Huntington's disease: the issue of intermediate and reduced penetrance allelesA Maat-Kievit, M Losekoot, H Van Den Boer-Van Den Berg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 23, 2000
Family history and DNA analysis in patients with suspected Huntington's diseaseS Siesling, M Vegter-van de Vlis, M Losekoot, et al.
Journal of Medical Genetics|November 3, 2004
A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15G J Breedveld, B van Wetten, G D te Raa, et al.
Journal of Medical Genetics|April 16, 1999
Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacitiesA T Helderman-van den Enden, P D Maaswinkel-Mooij, E Hoogendoorn, et al.
Journal of Medical Genetics|October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeB Horsthemke, A Maat-Kievit, E Sleegers, et al.
American Journal of Medical Genetics|January 23, 2002
Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington diseaseA Maat-Kievit, P Helderman-van den Enden, M Losekoot, et al.
Pageof 6