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Andrew P Read

Showing results (1-10 of 10) with videos related to

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Lancet (London, England)|August 21, 2003
How clinicians add to knowledge of developmentDian Donnai, Andrew P Read
Journal of Community Genetics|July 5, 2012
What can be offered to couples at (possibly) increased genetic risk?Andrew P Read, Dian Donnai
Trends in Molecular Medicine|September 13, 2005
Inherited eye disease: cause and late effectForbes D C Manson, Dorothy Trump, Andrew P Read, et al.
Human Molecular Genetics|November 22, 2002
SLUG (SNAI2) deletions in patients with Waardenburg diseaseManuel Sánchez-Martín, Arancha Rodríguez-García, Jesús Pérez-Losada, et al.
Human Molecular Genetics|May 23, 2002
Germline mutation of ARF in a melanoma kindredChelsee Hewitt, Chu Lee Wu, Gareth Evans, et al.
European Journal of Endocrinology|June 24, 2006
Phenotypic variation in constitutional delay of growth and puberty: relationship to specific leptin and leptin receptor gene polymorphismsIndraneel Banerjee, Julie A Trueman, Catherine M Hall, et al.
Cancer Letters|May 26, 2004
DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinomaChelsee Hewitt, Peter Wilson, Edwina McGlinn, et al.
The Journal of Clinical Endocrinology and Metabolism|November 18, 2004
Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: investigation of role in pubertal timingInes L Sedlmeyer, Celeste Leigh Pearce, Julie A Trueman, et al.
Science (New York, N.Y.)|November 19, 2005
GTF2IRD1 in craniofacial development of humans and miceMay Tassabehji, Peter Hammond, Annette Karmiloff-Smith, et al.
Human Mutation|February 20, 2004
The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitisChelsee Hewitt, Derek McCormick, Gerry Linden, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Lancet (London, England)|August 21, 2003
How clinicians add to knowledge of developmentDian Donnai, Andrew P Read
Journal of Community Genetics|July 5, 2012
What can be offered to couples at (possibly) increased genetic risk?Andrew P Read, Dian Donnai
Trends in Molecular Medicine|September 13, 2005
Inherited eye disease: cause and late effectForbes D C Manson, Dorothy Trump, Andrew P Read, et al.
Human Molecular Genetics|November 22, 2002
SLUG (SNAI2) deletions in patients with Waardenburg diseaseManuel Sánchez-Martín, Arancha Rodríguez-García, Jesús Pérez-Losada, et al.
Human Molecular Genetics|May 23, 2002
Germline mutation of ARF in a melanoma kindredChelsee Hewitt, Chu Lee Wu, Gareth Evans, et al.
European Journal of Endocrinology|June 24, 2006
Phenotypic variation in constitutional delay of growth and puberty: relationship to specific leptin and leptin receptor gene polymorphismsIndraneel Banerjee, Julie A Trueman, Catherine M Hall, et al.
Cancer Letters|May 26, 2004
DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinomaChelsee Hewitt, Peter Wilson, Edwina McGlinn, et al.
The Journal of Clinical Endocrinology and Metabolism|November 18, 2004
Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: investigation of role in pubertal timingInes L Sedlmeyer, Celeste Leigh Pearce, Julie A Trueman, et al.
Science (New York, N.Y.)|November 19, 2005
GTF2IRD1 in craniofacial development of humans and miceMay Tassabehji, Peter Hammond, Annette Karmiloff-Smith, et al.
Human Mutation|February 20, 2004
The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitisChelsee Hewitt, Derek McCormick, Gerry Linden, et al.
Pageof 1