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A P Smits

Showing results (11-20 of 26) with videos related to

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American Journal of Medical Genetics|April 1, 1992
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.
American Journal of Human Genetics|March 21, 2000
Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutationsR D Hundscheid, E A Sistermans, C M Thomas, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24A J van der Vleuten, C M van Ravenswaaij-Arts, C J Frijns, et al.
Human Genetics|March 1, 1993
DXS539, a polymorphic DNA marker proximal of the fragile-X geneJ C Dreesen, J A van den Hurk, A P Smits, et al.
American Journal of Medical Genetics|July 12, 1996
A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28B C Hamel, H Kremer, E Wesby-van Swaay, et al.
American Journal of Medical Genetics|July 15, 1994
Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptusesS L Sherman, A Maddalena, P N Howard-Peebles, et al.
Human Molecular Genetics|November 1, 1995
Normal phenotype in two brothers with a full FMR1 mutationH J Smeets, A P Smits, C E Verheij, et al.
Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.
American Journal of Medical Genetics|April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.
American Journal of Human Genetics|November 1, 1994
Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular dataB C Hamel, A P Smits, E de Graaff, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 1, 1992
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.
American Journal of Human Genetics|March 21, 2000
Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutationsR D Hundscheid, E A Sistermans, C M Thomas, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24A J van der Vleuten, C M van Ravenswaaij-Arts, C J Frijns, et al.
Human Genetics|March 1, 1993
DXS539, a polymorphic DNA marker proximal of the fragile-X geneJ C Dreesen, J A van den Hurk, A P Smits, et al.
American Journal of Medical Genetics|July 12, 1996
A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28B C Hamel, H Kremer, E Wesby-van Swaay, et al.
American Journal of Medical Genetics|July 15, 1994
Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptusesS L Sherman, A Maddalena, P N Howard-Peebles, et al.
Human Molecular Genetics|November 1, 1995
Normal phenotype in two brothers with a full FMR1 mutationH J Smeets, A P Smits, C E Verheij, et al.
Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.
American Journal of Medical Genetics|April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.
American Journal of Human Genetics|November 1, 1994
Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular dataB C Hamel, A P Smits, E de Graaff, et al.
Pageof 3