GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Molecular Cloning. A Laboratory Manual

1983 • 27,328 citations

Genomic sequencing.

1984 • 8,343 citations

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1990 • 1,300 citations

The GLI-Kruppel family of human genes.

1988 • 302 citations

Retinoids and vertebrate limb pattern formation

1989 • 251 citations

GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.

1990 • 180 citations

Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.

1988 • 73 citations

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

1983 • 69 citations

Chromosomal localisation of a developmental gene in man: Direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13

1988 • 58 citations

Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt)

1990 • 56 citations

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

1988 • 51 citations

Cellular oncogene activation

1989 • 47 citations

Cellular oncogene activation

1988 • 44 citations

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

1985 • 43 citations

Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13)

1989 • 34 citations

Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: Hemizygosity for PGAM2 and TCRG genes

1990 • 32 citations

Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13)

1989 • 31 citations

Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel

1990 • 8 citations