Search research articles
Contact Us
Filters
Showing results (1-10 of 8) with videos related to
Page
of 1
Sort By:
American Journal of Medical Genetics
|
October 3, 2002
Limb malformations and the human HOX genes
Frances R Goodman
Lancet (London, England)
|
August 29, 2003
Congenital abnormalities of body patterning: embryology revisited
Frances R Goodman
American Journal of Human Genetics
|
January 5, 2002
A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly
Frances 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 function
Giuliana Caronia, Frances R Goodman, Carole M E McKeown, et al.
Clinical Dysmorphology
|
March 15, 2006
Mild case of Curry-Jones syndrome
Ellen 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 syndrome
Jeffrey 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 families
Ravi Savarirayan, Susan M White, Frances R Goodman, et al.
American Journal of Medical Genetics
|
October 3, 2002
The mutational spectrum of brachydactyly type C
David B Everman, Cynthia F Bartels, Yue Yang, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics
|
October 3, 2002
Limb malformations and the human HOX genes
Frances R Goodman
Lancet (London, England)
|
August 29, 2003
Congenital abnormalities of body patterning: embryology revisited
Frances R Goodman
American Journal of Human Genetics
|
January 5, 2002
A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly
Frances 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 function
Giuliana Caronia, Frances R Goodman, Carole M E McKeown, et al.
Clinical Dysmorphology
|
March 15, 2006
Mild case of Curry-Jones syndrome
Ellen 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 syndrome
Jeffrey 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 families
Ravi Savarirayan, Susan M White, Frances R Goodman, et al.
American Journal of Medical Genetics
|
October 3, 2002
The mutational spectrum of brachydactyly type C
David B Everman, Cynthia F Bartels, Yue Yang, et al.
Page
of 1