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Biochemical and Biophysical Research Communications
|
November 25, 1998
Human myosin V gene produces different transcripts in a cell type-specific manner
J Lambert, J M Naeyaert, T Callens, et al.
Human Molecular Genetics
|
April 1, 1993
Lack of independence between five DNA polymorphisms in the NF1 gene
L Messiaen, S De Bie, T Moens, et al.
Cytogenetics and Cell Genetics
|
December 22, 1998
Assignment of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization
E De Baere, F Speleman, N Van Roy, et al.
Cytogenetics and Cell Genetics
|
December 22, 1998
Assignment of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25-->q26.1 by in situ hybridization
E De Baere, F Speleman, N Van Roy, et al.
American Journal of Medical Genetics
|
September 5, 1997
Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome
W Courtens, F Speleman, L Messiaen, et al.
Human Mutation
|
March 25, 1999
Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online
K Claes, E Machackova, M De Vos, et al.
Disease Markers
|
December 14, 1999
Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G
K Claes, E Machackova, M De Vos, et al.
American Journal of Medical Genetics. Part A
|
February 3, 2004
A new type of autosomal recessive spondyloepiphyseal dysplasia tarda
J G Leroy, B P Leroy, L V Emmery, et al.
BJU International
|
June 26, 2002
Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence
B Loeys, P Hoebeke, A Raes, et al.
Fertility and Sterility
|
February 6, 1999
Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the Automated Laser Fluorescence DNA Sequencer
K Sermon, W Lissens, L Messiaen, et al.
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Search research articles
Search
Showing results (11-20 of 57) with videos related to
Sort By:
Page
of 6
Biochemical and Biophysical Research Communications
|
November 25, 1998
Human myosin V gene produces different transcripts in a cell type-specific manner
J Lambert, J M Naeyaert, T Callens, et al.
Human Molecular Genetics
|
April 1, 1993
Lack of independence between five DNA polymorphisms in the NF1 gene
L Messiaen, S De Bie, T Moens, et al.
Cytogenetics and Cell Genetics
|
December 22, 1998
Assignment of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization
E De Baere, F Speleman, N Van Roy, et al.
Cytogenetics and Cell Genetics
|
December 22, 1998
Assignment of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25-->q26.1 by in situ hybridization
E De Baere, F Speleman, N Van Roy, et al.
American Journal of Medical Genetics
|
September 5, 1997
Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome
W Courtens, F Speleman, L Messiaen, et al.
Human Mutation
|
March 25, 1999
Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online
K Claes, E Machackova, M De Vos, et al.
Disease Markers
|
December 14, 1999
Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G
K Claes, E Machackova, M De Vos, et al.
American Journal of Medical Genetics. Part A
|
February 3, 2004
A new type of autosomal recessive spondyloepiphyseal dysplasia tarda
J G Leroy, B P Leroy, L V Emmery, et al.
BJU International
|
June 26, 2002
Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence
B Loeys, P Hoebeke, A Raes, et al.
Fertility and Sterility
|
February 6, 1999
Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the Automated Laser Fluorescence DNA Sequencer
K Sermon, W Lissens, L Messiaen, et al.
Page
of 6