Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM007439-17
Application #
2166548
Study Section
Genetic Basis of Disease Review Committee (GBD)
Project Start
1977-07-01
Project End
1997-06-30
Budget Start
1993-07-01
Budget End
1994-06-30
Support Year
17
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Yale University
Department
Genetics
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Hisama, F M; Zemel, S; Cherniske, E M et al. (2001) 46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters. Am J Med Genet 98:121-4
Hisama, F M; Reyes-Mugica, M; Wargowski, D S et al. (1998) Renal tubular dysgenesis, absent nipples, and multiple malformations in three brothers: a new, lethal syndrome. Am J Med Genet 80:335-42
Levanat, S; Gorlin, R J; Fallet, S et al. (1996) A two-hit model for developmental defects in Gorlin syndrome. Nat Genet 12:85-7
Yang-Feng, T L; Schneider, J W; Lindgren, V et al. (1988) Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes. Genomics 2:128-38
Keating, K M; Ghosaini, L R; Giedroc, D P et al. (1988) Thermal denaturation of T4 gene 32 protein: effects of zinc removal and substitution. Biochemistry 27:5240-5
Yang-Feng, T L; Barton, D E; Thelander, L et al. (1987) Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell lines. Genomics 1:77-86
Yang-Feng, T L; Landau, N R; Baltimore, D et al. (1986) The terminal deoxynucleotidyltransferase gene is located on human chromosome 10 (10q23----q24) and on mouse chromosome 19. Cytogenet Cell Genet 43:121-6
Yang-Feng, T L; Bruns, G A; Carroll, A J et al. (1986) Localization of the LDHA gene to 11p14----11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13. Hum Genet 74:331-4
Barton, D E; Yang-Feng, T L; Francke, U (1986) The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22----q24) by somatic cell hybrid analysis and in situ hybridization. Hum Genet 72:221-4
Lieberman, H B; Rabin, M; Barker, P E et al. (1985) Human metallothionein-II processed gene is located in region p11----q21 of chromosome 4. Cytogenet Cell Genet 39:109-15

Showing the most recent 10 out of 11 publications