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Human Genetics
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December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia
S Guioli, B Arveiler, B Bardoni, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1987
Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13
G de Saint Basile, B Arveiler, I Oberlé, et al.
Human Genetics
|
October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)
S Malcolm, G de Saint Basile, B Arveiler, et al.
Human Molecular Genetics
|
February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I
K L Evans, J Fantes, C Simpson, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2010
Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP gene
B Isidor, G Podevin, C Camby, et al.
Molecular Psychiatry
|
April 24, 2001
Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia
J K Millar, S Christie, S Anderson, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 16, 2008
Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African family
A Laleye, M J Alao, G Gbessi, et al.
Ophthalmic Genetics
|
September 13, 2022
Foveal hypoplasia in parents of patients with albinism
R Lejoyeux, A-S Alonso, J Lafolie, et al.
Clinical Genetics
|
August 23, 2006
Mosaic maternal uniparental isodisomy for chromosome 7q21-qter
M-P Reboul, O Tandonnet, N Biteau, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 27, 2021
Management of albinism: French guidelines for diagnosis and care
E Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 64) with videos related to
Sort By:
Page
of 7
Human Genetics
|
December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia
S Guioli, B Arveiler, B Bardoni, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1987
Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13
G de Saint Basile, B Arveiler, I Oberlé, et al.
Human Genetics
|
October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)
S Malcolm, G de Saint Basile, B Arveiler, et al.
Human Molecular Genetics
|
February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I
K L Evans, J Fantes, C Simpson, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2010
Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP gene
B Isidor, G Podevin, C Camby, et al.
Molecular Psychiatry
|
April 24, 2001
Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia
J K Millar, S Christie, S Anderson, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 16, 2008
Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African family
A Laleye, M J Alao, G Gbessi, et al.
Ophthalmic Genetics
|
September 13, 2022
Foveal hypoplasia in parents of patients with albinism
R Lejoyeux, A-S Alonso, J Lafolie, et al.
Clinical Genetics
|
August 23, 2006
Mosaic maternal uniparental isodisomy for chromosome 7q21-qter
M-P Reboul, O Tandonnet, N Biteau, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 27, 2021
Management of albinism: French guidelines for diagnosis and care
E Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.
Page
of 7