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A P Read

Nature genetics

Showing results (1-10 of 8) with videos related to

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Nature Genetics|August 1, 1993
Huntington's disease: testing the testA P Read
Nature Genetics|April 1, 1995
Pax genes--paired feet in three campsA P Read
Nature Genetics|November 1, 1994
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) geneM Tassabehji, V E Newton, A P Read
Nature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
Nature Genetics|July 1, 1996
LIM-kinase deleted in Williams syndromeM Tassabehji, K Metcalfe, W D Fergusson, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
Nature Genetics|December 2, 1999
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosisC Toomes, J James, A J Wood, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Nature Genetics|August 1, 1993
Huntington's disease: testing the testA P Read
Nature Genetics|April 1, 1995
Pax genes--paired feet in three campsA P Read
Nature Genetics|November 1, 1994
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) geneM Tassabehji, V E Newton, A P Read
Nature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
Nature Genetics|July 1, 1996
LIM-kinase deleted in Williams syndromeM Tassabehji, K Metcalfe, W D Fergusson, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
Nature Genetics|December 2, 1999
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosisC Toomes, J James, A J Wood, et al.
Pageof 1