Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Program Projects (P01)
Project #
8P01HG000373-03
Application #
3097339
Study Section
Special Emphasis Panel (SSS (D))
Project Start
1988-09-29
Project End
1993-08-31
Budget Start
1990-09-01
Budget End
1991-08-31
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Agarwala, R; Biesecker, L G; Hopkins, K A et al. (1998) Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster County. Genome Res 8:211-21
Polymeropoulos, M H; Ide, S E; Wright, M et al. (1996) The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16. Genomics 35:1-5
Bellus, G A; Hefferon, T W; Ortiz de Luna, R I et al. (1995) Achondroplasia is defined by recurrent G380R mutations of FGFR3. Am J Hum Genet 56:368-73
Drebin, J A; Hartzell, S W; Griffin, C et al. (1995) Molecular cloning and chromosomal localization of the human homologue of a B-lymphocyte specific protein tyrosine kinase (blk). Oncogene 10:477-86
Hecht, J T; Herrera, C A; Greenhaw, G A et al. (1995) Confirmatory linkage of hypochondroplasia to chromosome arm 4p. Am J Med Genet 57:505-6
Greenspan, D S; Northrup, H; Au, K S et al. (1995) COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type II. Genomics 25:737-9
Cabin, D E; Hawkins, A; Griffin, C et al. (1995) YAC transgenic mice in the study of the genetic basis of Down syndrome. Prog Clin Biol Res 393:213-26
Carow, C E; Kim, E; Hawkins, A L et al. (1995) Localization of the human stem cell tyrosine kinase-1 gene (FLT3) to 13q12-->q13. Cytogenet Cell Genet 70:255-7
Malo, M S; Blanchard, B J; Andresen, J M et al. (1994) Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24. Cytogenet Cell Genet 67:178-86
Sulisalo, T; Klockars, J; Makitie, O et al. (1994) High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene. Am J Hum Genet 55:937-45

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