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Showing results (51-60 of 76) with videos related to

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American Journal of Human Genetics|January 13, 2000
Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndromeD Monk, E L Wakeling, V Proud, et al.
Journal of Dental Research|January 1, 2010
Autosomal-dominant ankyloglossia and tooth number anomaliesA C Acevedo, J A C da Fonseca, J Grinham, et al.
Journal of Medical Genetics|June 30, 2000
An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probandsM A Preece, S N Abu-Amero, Z Ali, et al.
Diabetes|January 9, 2001
Evidence that insulin is imprinted in the human yolk sacG E Moore, S N Abu-Amero, G Bell, et al.
Cytogenetics and Cell Genetics|March 7, 2000
Report of the fifth international workshop on human chromosome 1 mapping 1999P S White, A Forus, T C Matise, et al.
Journal of Dental Research|January 21, 2011
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutationsP N Kantaputra, M Paramee, A Kaewkhampa, et al.
Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.
Nature Genetics|September 18, 2001
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.
American Journal of Medical Genetics. Part A|June 14, 2005
Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patientsK Doudney, P Ybot-Gonzalez, C Paternotte, et al.
Lancet (London, England)|November 30, 1985
Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implicationsP J Scambler, B J Wainwright, M Farrall, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|January 13, 2000
Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndromeD Monk, E L Wakeling, V Proud, et al.
Journal of Dental Research|January 1, 2010
Autosomal-dominant ankyloglossia and tooth number anomaliesA C Acevedo, J A C da Fonseca, J Grinham, et al.
Journal of Medical Genetics|June 30, 2000
An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probandsM A Preece, S N Abu-Amero, Z Ali, et al.
Diabetes|January 9, 2001
Evidence that insulin is imprinted in the human yolk sacG E Moore, S N Abu-Amero, G Bell, et al.
Cytogenetics and Cell Genetics|March 7, 2000
Report of the fifth international workshop on human chromosome 1 mapping 1999P S White, A Forus, T C Matise, et al.
Journal of Dental Research|January 21, 2011
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutationsP N Kantaputra, M Paramee, A Kaewkhampa, et al.
Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.
Nature Genetics|September 18, 2001
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.
American Journal of Medical Genetics. Part A|June 14, 2005
Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patientsK Doudney, P Ybot-Gonzalez, C Paternotte, et al.
Lancet (London, England)|November 30, 1985
Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implicationsP J Scambler, B J Wainwright, M Farrall, et al.
Pageof 8