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Lancet (London, England)
|
August 21, 2003
How clinicians add to knowledge of development
Dian 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 effect
Forbes D C Manson, Dorothy Trump, Andrew P Read, et al.
Human Molecular Genetics
|
November 22, 2002
SLUG (SNAI2) deletions in patients with Waardenburg disease
Manuel Sánchez-Martín, Arancha Rodríguez-García, Jesús Pérez-Losada, et al.
Human Molecular Genetics
|
May 23, 2002
Germline mutation of ARF in a melanoma kindred
Chelsee 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 polymorphisms
Indraneel 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 carcinoma
Chelsee 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 timing
Ines 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 mice
May 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 periodontitis
Chelsee Hewitt, Derek McCormick, Gerry Linden, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Lancet (London, England)
|
August 21, 2003
How clinicians add to knowledge of development
Dian 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 effect
Forbes D C Manson, Dorothy Trump, Andrew P Read, et al.
Human Molecular Genetics
|
November 22, 2002
SLUG (SNAI2) deletions in patients with Waardenburg disease
Manuel Sánchez-Martín, Arancha Rodríguez-García, Jesús Pérez-Losada, et al.
Human Molecular Genetics
|
May 23, 2002
Germline mutation of ARF in a melanoma kindred
Chelsee 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 polymorphisms
Indraneel 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 carcinoma
Chelsee 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 timing
Ines 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 mice
May 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 periodontitis
Chelsee Hewitt, Derek McCormick, Gerry Linden, et al.
Page
of 1