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P Stanier

Showing results (31-40 of 76) with videos related to

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Genomics|September 1, 1993
The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1XP Stanier, S A Forbes, A Arnason, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissuesE L Wakeling, S N Abu-Amero, P Stanier, et al.
Cytogenetics and Cell Genetics|October 9, 1998
Linkage mapping of Lims1l, the murine homolog of the human LIM domain gene PINCH, to mouse chromosome 10S Abu-Hayyeh, J Eddleston, J N Murdoch, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
The search for the gene for Silver-Russell syndromeG E Moore, S Abu-Amero, E Wakeling, et al.
Genomics|June 13, 2001
Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23K Doudney, J N Murdoch, C Paternotte, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver Russell syndrome probands and their familiesS Abu-Amero, S Price, E Wakeling, et al.
Human Genetics|March 1, 1995
Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindredS A Forbes, M Richardson, L Brennan, et al.
Prenatal Diagnosis|March 1, 1987
Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probesH Y Law, P Stanier, R Williamson, et al.
Journal of Medical Genetics|August 6, 2002
Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndromeD Monk, L Bentley, C Beechey, et al.
Journal of Medical Genetics|March 19, 2002
Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17qM P Hitchins, S Abu-Amero, S Apostolidou, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
Genomics|September 1, 1993
The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1XP Stanier, S A Forbes, A Arnason, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissuesE L Wakeling, S N Abu-Amero, P Stanier, et al.
Cytogenetics and Cell Genetics|October 9, 1998
Linkage mapping of Lims1l, the murine homolog of the human LIM domain gene PINCH, to mouse chromosome 10S Abu-Hayyeh, J Eddleston, J N Murdoch, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
The search for the gene for Silver-Russell syndromeG E Moore, S Abu-Amero, E Wakeling, et al.
Genomics|June 13, 2001
Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23K Doudney, J N Murdoch, C Paternotte, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver Russell syndrome probands and their familiesS Abu-Amero, S Price, E Wakeling, et al.
Human Genetics|March 1, 1995
Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindredS A Forbes, M Richardson, L Brennan, et al.
Prenatal Diagnosis|March 1, 1987
Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probesH Y Law, P Stanier, R Williamson, et al.
Journal of Medical Genetics|August 6, 2002
Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndromeD Monk, L Bentley, C Beechey, et al.
Journal of Medical Genetics|March 19, 2002
Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17qM P Hitchins, S Abu-Amero, S Apostolidou, et al.
Pageof 8