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3 in total

1. Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors: Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal: Science Date: 1987-03-27 Impact factor: 47.728

2. Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19.

Authors: S Naylor; J M Lalouel; D J Shaw
Journal: Cytogenet Cell Genet Date: 1985

3. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors: G M Lathrop; J M Lalouel; C Julier; J Ott
Journal: Am J Hum Genet Date: 1985-05 Impact factor: 11.025

3 in total

1. An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance.

Authors: C Hayward; J Livingstone; S Holloway; W A Liston; D J Brock
Journal: Am J Hum Genet Date: 1992-04 Impact factor: 11.025

2. Identification of complex DNA polymorphisms based on variable number of tandem repeats (VNTR) and restriction site polymorphism.

Authors: J S Waye; R M Fourney
Journal: Hum Genet Date: 1990-02 Impact factor: 4.132

3. Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.

Authors: D Trump; M P Whyte; C Wooding; J T Pang; S H Pearce; D B Kocher; R V Thakker
Journal: Hum Genet Date: 1995-08 Impact factor: 4.132

3 in total