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P Stanier

Showing results (41-50 of 76) with videos related to

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Genomics|November 15, 2001
Circletail, a new mouse mutant with severe neural tube defects: chromosomal localization and interaction with the loop-tail mutationJ N Murdoch, R A Rachel, S Shah, et al.
Journal of Medical Genetics|January 1, 1997
Maternal uniparental disomy 7 in Silver-Russell syndromeM A Preece, S M Price, V Davies, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndromeM P Hitchins, D Monk, G M Bell, et al.
Journal of Medical Genetics|February 26, 2000
Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndromeE L Wakeling, M P Hitchins, S N Abu-Amero, et al.
Genomics|June 13, 2001
Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical regionC Braybrook, G Warry, G Howell, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 2006
Limited evolutionary conservation of imprinting in the human placentaD Monk, P Arnaud, S Apostolidou, et al.
Clinical Genetics|May 1, 1994
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defectsR Newton, P Stanier, S Loughna, et al.
Human Genetics|August 14, 2001
Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical regionC Braybrook, G Warry, G Howell, et al.
Progress in Clinical and Biological Research|January 1, 1987
The application of molecular genetics to the study of the basic defect causing cystic fibrosisX Estivill, G Bates, G Bell, et al.
Hormone Research|September 8, 1998
Genetics of Silver-Russell syndromeE L Wakeling, S Abu-Amero, S M Price, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Genomics|November 15, 2001
Circletail, a new mouse mutant with severe neural tube defects: chromosomal localization and interaction with the loop-tail mutationJ N Murdoch, R A Rachel, S Shah, et al.
Journal of Medical Genetics|January 1, 1997
Maternal uniparental disomy 7 in Silver-Russell syndromeM A Preece, S M Price, V Davies, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndromeM P Hitchins, D Monk, G M Bell, et al.
Journal of Medical Genetics|February 26, 2000
Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndromeE L Wakeling, M P Hitchins, S N Abu-Amero, et al.
Genomics|June 13, 2001
Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical regionC Braybrook, G Warry, G Howell, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 2006
Limited evolutionary conservation of imprinting in the human placentaD Monk, P Arnaud, S Apostolidou, et al.
Clinical Genetics|May 1, 1994
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defectsR Newton, P Stanier, S Loughna, et al.
Human Genetics|August 14, 2001
Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical regionC Braybrook, G Warry, G Howell, et al.
Progress in Clinical and Biological Research|January 1, 1987
The application of molecular genetics to the study of the basic defect causing cystic fibrosisX Estivill, G Bates, G Bell, et al.
Hormone Research|September 8, 1998
Genetics of Silver-Russell syndromeE L Wakeling, S Abu-Amero, S M Price, et al.
Pageof 8