Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Program Projects (P01)
Project #
5P01HG000373-05
Application #
3097338
Study Section
Special Emphasis Panel (SSS (D))
Project Start
1988-09-29
Project End
1993-08-31
Budget Start
1992-09-01
Budget End
1993-08-31
Support Year
5
Fiscal Year
1992
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
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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
Narayanan, V; Ripepi, B; Jabs, E W et al. (1994) Partial structure and mapping of the human myelin P2 protein gene. J Neurochem 63:2010-3
Zappata, S; Petersen, M B; Konig, U et al. (1994) Highly polymorphic repeat marker within the beta-amyloid precursor protein gene. Hum Genet 93:85-6

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