Concepedia

G D Billingsley

GD

Statistics

Publications

9

Citations

518

H-Index

9

Active since

1984

Affiliations

Hospital for Sick Children(Current)

University of Toronto

G D Billingsley is an author at Hospital for Sick Children specializing in life sciences, genetics, and molecular genetics.

Publications per year

1984–2010

9

Publications

9

Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.

D Gill, R. Klose, Francis L. Munier et al. · PubMed · 2000 · 150 citations

, , +17

Physical mapping of four serpin genes: alpha 1-antitrypsin, alpha 1-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280-kb region on chromosome I4q32.1.

G D Billingsley, Michele Walter, Geoffrey L. Hammond et al. · PubMed · 1993 · 99 citations

, , +6

Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population

G D Billingsley, Jenea M. Bin, Karen Fieggen et al. · Journal of Medical Genetics · 2010 · 90 citations

, , +14

Aggregation of plasma Z type α<sub>1</sub>‐antitrypsin suggests basic defect for the deficiency

D W Cox, G D Billingsley, John W. Callahan · FEBS Letters · 1986 · 49 citations · Full text

, , +14

X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.

Jennifer MacKenzie, Jennifer M. Fitzpatrick, Paul Babyn et al. · Journal of Medical Genetics · 1996 · 38 citations · Full text

, , +16

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