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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 disease
G 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 disease
G 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 gestation
J 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 alleles
A 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 disease
S 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 11p15
G 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 capacities
A 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 syndrome
B 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 disease
A Maat-Kievit, P Helderman-van den Enden, M Losekoot, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 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 disease
G 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 disease
G 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 gestation
J 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 alleles
A 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 disease
S 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 11p15
G 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 capacities
A 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 syndrome
B 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 disease
A Maat-Kievit, P Helderman-van den Enden, M Losekoot, et al.
Page
of 6