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K L Greenhalgh

Showing results (1-10 of 7) with videos related to

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Familial Cancer|February 1, 2008
Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutationH R Murphy, R Armstrong, D Cairns, et al.
Journal of Medical Genetics|March 3, 2009
Succinate dehydrogenase subunit B (SDHB) gene deletion associated with a composite paraganglioma/neuroblastomaR Armstrong, K L Greenhalgh, E Rattenberry, et al.
Clinical Dysmorphology|January 7, 2003
Siblings with Bohring-Opitz syndromeK L Greenhalgh, R A Newbury-Ecob, P W Lunt, et al.
The British Journal of Ophthalmology|April 26, 2003
Novel corneal features in two males with incontinentia pigmentiE J Mayer, G N Shuttleworth, K L Greenhalgh, et al.
Archives of Disease in Childhood|May 27, 2003
22q11 deletion: a multisystem disorder requiring multidisciplinary inputK L Greenhalgh, I A Aligianis, G Bromilow, et al.
Archives of Disease in Childhood|May 24, 2008
Phaeochromocytoma in childrenR Armstrong, M Sridhar, K L Greenhalgh, et al.
Journal of Medical Genetics|December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic studyK L Greenhalgh, R T Howell, A Bottani, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Familial Cancer|February 1, 2008
Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutationH R Murphy, R Armstrong, D Cairns, et al.
Journal of Medical Genetics|March 3, 2009
Succinate dehydrogenase subunit B (SDHB) gene deletion associated with a composite paraganglioma/neuroblastomaR Armstrong, K L Greenhalgh, E Rattenberry, et al.
Clinical Dysmorphology|January 7, 2003
Siblings with Bohring-Opitz syndromeK L Greenhalgh, R A Newbury-Ecob, P W Lunt, et al.
The British Journal of Ophthalmology|April 26, 2003
Novel corneal features in two males with incontinentia pigmentiE J Mayer, G N Shuttleworth, K L Greenhalgh, et al.
Archives of Disease in Childhood|May 27, 2003
22q11 deletion: a multisystem disorder requiring multidisciplinary inputK L Greenhalgh, I A Aligianis, G Bromilow, et al.
Archives of Disease in Childhood|May 24, 2008
Phaeochromocytoma in childrenR Armstrong, M Sridhar, K L Greenhalgh, et al.
Journal of Medical Genetics|December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic studyK L Greenhalgh, R T Howell, A Bottani, et al.
Pageof 1