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Human Mutation
|
January 1, 1993
Identification of mutations in Danish choroideremia families
M Schwartz, T Rosenberg, J A van den Hurk, et al.
Nucleic Acids Research
|
March 25, 1992
Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2
C M Molloy, T J van de Pol, R M Brohet, et al.
Human Genetics
|
November 10, 2001
DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements
R Kirschner, D Erturk, C Zeitz, et al.
Human Reproduction (Oxford, England)
|
October 21, 1999
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?
Y M van Kasteren, R D Hundscheid, A P Smits, et al.
Human Genetics
|
August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation
H Traupe, D Müller, D Atherton, et al.
Human Molecular Genetics
|
December 6, 2001
CRB1 has a cytoplasmic domain that is functionally conserved between human and Drosophila
A I den Hollander, K Johnson, Y J de Kok, et al.
Human Genetics
|
March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism
H Traupe, U Vetter, R Happle, et al.
The British Journal of Ophthalmology
|
July 22, 1999
Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene
B J Klevering, M van Driel, D J van de Pol, et al.
Clinical Genetics
|
December 1, 1987
Deletion of the DXS165 locus in patients with classical choroideremia
F P Cremers, F Brunsmann, T J van de Pol, et al.
Ophthalmic Genetics
|
September 1, 1996
A highly polymorphic microsatellite marker located within the choroideremia gene
H Van Bokhoven, J A Van den Hurk, L Bogerd, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 80) with videos related to
Sort By:
Page
of 8
Human Mutation
|
January 1, 1993
Identification of mutations in Danish choroideremia families
M Schwartz, T Rosenberg, J A van den Hurk, et al.
Nucleic Acids Research
|
March 25, 1992
Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2
C M Molloy, T J van de Pol, R M Brohet, et al.
Human Genetics
|
November 10, 2001
DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements
R Kirschner, D Erturk, C Zeitz, et al.
Human Reproduction (Oxford, England)
|
October 21, 1999
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?
Y M van Kasteren, R D Hundscheid, A P Smits, et al.
Human Genetics
|
August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation
H Traupe, D Müller, D Atherton, et al.
Human Molecular Genetics
|
December 6, 2001
CRB1 has a cytoplasmic domain that is functionally conserved between human and Drosophila
A I den Hollander, K Johnson, Y J de Kok, et al.
Human Genetics
|
March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism
H Traupe, U Vetter, R Happle, et al.
The British Journal of Ophthalmology
|
July 22, 1999
Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene
B J Klevering, M van Driel, D J van de Pol, et al.
Clinical Genetics
|
December 1, 1987
Deletion of the DXS165 locus in patients with classical choroideremia
F P Cremers, F Brunsmann, T J van de Pol, et al.
Ophthalmic Genetics
|
September 1, 1996
A highly polymorphic microsatellite marker located within the choroideremia gene
H Van Bokhoven, J A Van den Hurk, L Bogerd, et al.
Page
of 8