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Frances R Goodman

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

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American Journal of Medical Genetics|October 3, 2002
Limb malformations and the human HOX genesFrances R Goodman
Lancet (London, England)|August 29, 2003
Congenital abnormalities of body patterning: embryology revisitedFrances R Goodman
American Journal of Human Genetics|January 5, 2002
A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactylyFrances R Goodman, Frank Majewski, Amanda L Collins, et al.
Development (Cambridge, England)|March 7, 2003
An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of functionGiuliana Caronia, Frances R Goodman, Carole M E McKeown, et al.
Clinical Dysmorphology|March 15, 2006
Mild case of Curry-Jones syndromeEllen R A Thomas, Emma L Wakeling, Frances R Goodman, et al.
Human Mutation|April 23, 2002
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndromeJeffrey W Innis, Frances R Goodman, Chiara Bacchelli, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated familiesRavi Savarirayan, Susan M White, Frances R Goodman, et al.
American Journal of Medical Genetics|October 3, 2002
The mutational spectrum of brachydactyly type CDavid B Everman, Cynthia F Bartels, Yue Yang, et al.
Pageof 1

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

Sort By:
Pageof 1
American Journal of Medical Genetics|October 3, 2002
Limb malformations and the human HOX genesFrances R Goodman
Lancet (London, England)|August 29, 2003
Congenital abnormalities of body patterning: embryology revisitedFrances R Goodman
American Journal of Human Genetics|January 5, 2002
A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactylyFrances R Goodman, Frank Majewski, Amanda L Collins, et al.
Development (Cambridge, England)|March 7, 2003
An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of functionGiuliana Caronia, Frances R Goodman, Carole M E McKeown, et al.
Clinical Dysmorphology|March 15, 2006
Mild case of Curry-Jones syndromeEllen R A Thomas, Emma L Wakeling, Frances R Goodman, et al.
Human Mutation|April 23, 2002
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndromeJeffrey W Innis, Frances R Goodman, Chiara Bacchelli, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated familiesRavi Savarirayan, Susan M White, Frances R Goodman, et al.
American Journal of Medical Genetics|October 3, 2002
The mutational spectrum of brachydactyly type CDavid B Everman, Cynthia F Bartels, Yue Yang, et al.
Pageof 1