Publications by authors named "Frances R Goodman"

Claim this Profile
M
Mild case of Curry-Jones syndrome.
Ellen R A Thomas, Emma L Wakeling, Frances R Goodman, John C Dickinson, Christine M Hall

Clin Dysmorphol· April 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital abnormalities of body patterning: embryology revisited.
Frances R Goodman

Lancet· August 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
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, Peter J Scambler, Vincenzo Zappavigna

Development· April 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families.
Ravi Savarirayan, Susan M White, Frances R Goodman, John M Graham, Martin B Delatycki

Am J Med Genet A· March 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Limb malformations and the human HOX genes.
Frances R Goodman

Am J Med Genet· October 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The mutational spectrum of brachydactyly type C.
David B Everman, Cynthia F Bartels, Yue Yang, Niranjan Yanamandra, Frances R Goodman

Am J Med Genet· October 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
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, Thomas M Williams, Douglas P Mortlock

Hum Mutat· May 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly.
Frances R Goodman, Frank Majewski, Amanda L Collins, Peter J Scambler

Am J Hum Genet· February 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis