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Showing 1–11 of 11 results

Advanced filters: Author: Murray Feingold Clear advanced filters

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

Elena V. Semina
Rebecca Reiter
Jeffrey C. Murray
Research01 Dec 1996
Nature Genetics

Volume: 14, P: 392-399
489 MEDICAL STUDENTS AND THE DECISION MAKING PROCESS

Murray Feingold
Research01 Apr 1978
Pediatric Research

Volume: 12, P: 445
QUANTITATIVE EVALUATION OF ABNORMAL FEATURES IN SELECTED SYNDROMES

Marilyn Preus
F Clarke Fraser
Murray Feingold
Research01 Apr 1974
Pediatric Research

Volume: 8, P: 441
What's in a name?

Murray Feingold
Correspondence01 May 1999
Genetics in Medicine

Volume: 1, P: 170
Mutations in the pre-replication complex cause Meier-Gorlin syndrome

Andrew Jackson, Ernie Bongers and colleagues report the identification of mutations in five genes in individuals with Meier-Gorlin syndrome. The five genes, ORC1, ORC4, ORC6, CDT1 and CDC6, all encode components of the pre-replication complex.

Louise S Bicknell
Ernie M H F Bongers
Andrew P Jackson
Research27 Feb 2011
Nature Genetics

Volume: 43, P: 356-359
Detectable clonal mosaicism from birth to old age and its relationship to cancer

Cathy Laurie and colleagues detect mosaicism for large chromosomal abnormalities in peripheral blood in a subset of healthy individuals. They show that the frequency of such events increases with age and is associated with elevated risk of developing a subsequent hematological cancer.

Cathy C Laurie
Cecelia A Laurie
Bruce S Weir
Research06 May 2012
Nature Genetics

Volume: 44, P: 642-650
Co-selection for antibiotic resistance by environmental contaminants

Laura May Murray
April Hayes
Aimee Kaye Murray
ReviewsOpen Access01 Apr 2024
npj Antimicrobials and Resistance

Volume: 2, P: 1-13
292 A Genome-Wide Association Study of Spontaneous Preterm Delivery

H Boyd
B Feenstra
Geneva Consortium
Research01 Nov 2010
Pediatric Research

Volume: 68, P: 150
No observed association for mitochondrial SNPs with preterm delivery and related outcomes

Brandon W. Alleman
Solveig Myking
Jeffrey C. Murray
Research17 Aug 2012
Pediatric Research

Volume: 72, P: 539-544
PROXIMAL 15q DELETION IN A FATHER AND SON WITH ISOLATED OBESITY

Jane E O'Brien
Murray Feingold
Wayne A Miller
Research01 Apr 1987
Pediatric Research

Volume: 21, P: 229
Meier–Gorlin syndrome genotype–phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis

Sonja A de Munnik
Louise S Bicknell
Ernie M H F Bongers
Research15 Feb 2012
European Journal of Human Genetics

Volume: 20, P: 598-606