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Neil V Whittock

Showing results (1-10 of 12) with videos related to

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Advances in Experimental Medicine and Biology|November 3, 2010
Somitogenesis. PrefaceMiguel Maroto, Neil V Whittock
The Journal of Investigative Dermatology|March 22, 2003
Genetic evidence for a novel human desmosomal cadherin, desmoglein 4Neil V Whittock, Christopher Bower
Prenatal Diagnosis|July 18, 2003
Molecular genetic prenatal diagnosis for a case of autosomal recessive spondylocostal dysostosisNeil V Whittock, Peter D Turnpenny, Joep Tuerlings, et al.
The Journal of Clinical Investigation|November 17, 2004
Defining the pathogenic involvement of desmoglein 4 in pemphigus and staphylococcal scalded skin syndromeTakeshi Nagasaka, Koji Nishifuji, Takayuki Ota, et al.
American Journal of Human Genetics|May 4, 2004
Mutated MESP2 causes spondylocostal dysostosis in humansNeil V Whittock, Duncan B Sparrow, Merridee A Wouters, et al.
The Journal of Investigative Dermatology|September 17, 2002
Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genesEli Sprecher, Peter Itin, Neil V Whittock, et al.
The Journal of Investigative Dermatology|November 25, 2003
Novel mutations in X-linked dominant chondrodysplasia punctata (CDPX2)Neil V Whittock, Louise Izatt, Anuska Mann, et al.
The Journal of Investigative Dermatology|May 2, 2002
Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratodermaNeil V Whittock, Frances J Smith, Hong Wan, et al.
The Journal of Investigative Dermatology|August 8, 2002
Defolliculated (dfl): a dominant mouse mutation leading to poor sebaceous gland differentiation and total elimination of pelage folliclesRebecca M Porter, Colin A B Jahoda, Declan P Lunny, et al.
The Journal of Investigative Dermatology|February 14, 2002
Compound heterozygosity for non-sense and mis-sense mutations in desmoplakin underlies skin fragility/woolly hair syndromeNeil V Whittock, Hong Wan, Susan M Morley, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|November 3, 2010
Somitogenesis. PrefaceMiguel Maroto, Neil V Whittock
The Journal of Investigative Dermatology|March 22, 2003
Genetic evidence for a novel human desmosomal cadherin, desmoglein 4Neil V Whittock, Christopher Bower
Prenatal Diagnosis|July 18, 2003
Molecular genetic prenatal diagnosis for a case of autosomal recessive spondylocostal dysostosisNeil V Whittock, Peter D Turnpenny, Joep Tuerlings, et al.
The Journal of Clinical Investigation|November 17, 2004
Defining the pathogenic involvement of desmoglein 4 in pemphigus and staphylococcal scalded skin syndromeTakeshi Nagasaka, Koji Nishifuji, Takayuki Ota, et al.
American Journal of Human Genetics|May 4, 2004
Mutated MESP2 causes spondylocostal dysostosis in humansNeil V Whittock, Duncan B Sparrow, Merridee A Wouters, et al.
The Journal of Investigative Dermatology|September 17, 2002
Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genesEli Sprecher, Peter Itin, Neil V Whittock, et al.
The Journal of Investigative Dermatology|November 25, 2003
Novel mutations in X-linked dominant chondrodysplasia punctata (CDPX2)Neil V Whittock, Louise Izatt, Anuska Mann, et al.
The Journal of Investigative Dermatology|May 2, 2002
Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratodermaNeil V Whittock, Frances J Smith, Hong Wan, et al.
The Journal of Investigative Dermatology|August 8, 2002
Defolliculated (dfl): a dominant mouse mutation leading to poor sebaceous gland differentiation and total elimination of pelage folliclesRebecca M Porter, Colin A B Jahoda, Declan P Lunny, et al.
The Journal of Investigative Dermatology|February 14, 2002
Compound heterozygosity for non-sense and mis-sense mutations in desmoplakin underlies skin fragility/woolly hair syndromeNeil V Whittock, Hong Wan, Susan M Morley, et al.
Pageof 2