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S Malcolm

Showing results (211-220 of 271) with videos related to

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Allergologia Et Immunopathologia|January 1, 1991
Gene therapy for X-linked immunodeficienciesC Kinnon, M A O'Reilly, A Pelham, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 27, 2000
Plasma proteins modified by tyrosine nitration in acute respiratory distress syndromeM D Gole, J M Souza, I Choi, et al.
Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.
Clinical Genetics|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, et al.
Human Molecular Genetics|August 1, 1994
Localization of the genetic locus for Saethre-Chotzen syndrome to a 6 cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2C S Rose, A A King, D Summers, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Molecular Microbiology|September 3, 2011
Chlamydia trachomatis Slc1 is a type III secretion chaperone that enhances the translocation of its invasion effector substrate TARPAmanda J Brinkworth, Denise S Malcolm, António T Pedrosa, et al.
Human Molecular Genetics|November 1, 1995
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 geneY J de Kok, G F Merkx, S M van der Maarel, et al.
Prenatal Diagnosis|July 1, 1989
Rapid sexing of human embryos by non-radioactive in situ hybridization: potential for preimplantation diagnosis of X-linked disordersR J Penketh, J D Delhanty, J A van den Berghe, et al.
Pageof 28

Showing results (211-220 of 271) with videos related to

Sort By:
Pageof 28
Allergologia Et Immunopathologia|January 1, 1991
Gene therapy for X-linked immunodeficienciesC Kinnon, M A O'Reilly, A Pelham, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 27, 2000
Plasma proteins modified by tyrosine nitration in acute respiratory distress syndromeM D Gole, J M Souza, I Choi, et al.
Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.
Clinical Genetics|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, et al.
Human Molecular Genetics|August 1, 1994
Localization of the genetic locus for Saethre-Chotzen syndrome to a 6 cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2C S Rose, A A King, D Summers, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Molecular Microbiology|September 3, 2011
Chlamydia trachomatis Slc1 is a type III secretion chaperone that enhances the translocation of its invasion effector substrate TARPAmanda J Brinkworth, Denise S Malcolm, António T Pedrosa, et al.
Human Molecular Genetics|November 1, 1995
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 geneY J de Kok, G F Merkx, S M van der Maarel, et al.
Prenatal Diagnosis|July 1, 1989
Rapid sexing of human embryos by non-radioactive in situ hybridization: potential for preimplantation diagnosis of X-linked disordersR J Penketh, J D Delhanty, J A van den Berghe, et al.
Pageof 28