Greig cephalopolysyndactyly syndrome: A possible mouse homologue (Xt‐extra toes)

Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7

1985 • 205 citations

Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.

1967 • 172 citations

Chromosome maps of man and mouse, III

1987 • 162 citations

Chromosomal Locations of the Murine T-Cell Receptor Alpha-Chain Gene and the T-Cell Gamma Gene

1985 • 95 citations

A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly‐craniofacial anomalies syndrome

1983 • 69 citations

Malformation syndromes: a review of mouse/human homology.

1988 • 46 citations

The Greig cephalopolysyndactyly syndrome: Report of a family and review of the literature

1985 • 43 citations

Greig cephalopolysyndactyly: report of 13 affected individuals in three families

1983 • 41 citations

Frontonasal dysplasia, coronal cranisoynostosis, pre‐ and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression?

1983 • 36 citations

Familial polysyndactyly and craniofacial anomalies

1972 • 32 citations

Greig Cephalopolysyndactyly Syndrome

1979 • 30 citations

Brachyphalangy, an allele of extra-toes in the mouse

1969 • 30 citations

Frontodigital syndrome: A dominantly inherited disorder with normal intelligence

1970 • 28 citations

A NEWBORN INFANT WITH CRANIOFACIAL DYSMORPHISM AND POLYSYNDACTYLY (GREIG'S SYNDROME)

1981 • 22 citations

The greig cephalopolysyndactyly syndrome in a canadian family

1982 • 19 citations

The Greig polysyndactyly craniofacial dysmorphism syndrome.

1980 • 17 citations

The Greig polysyndactyly-craniofacial dysmorphism syndrome

1977 • 16 citations

The Greig polysyndactyly craniofacial dysmorphism syndrome: Variable expression in a family

1981 • 14 citations

Greig cephalopolysyndactyly syndrome. Report of a sporadic case.

1985 • 12 citations