Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29DE009954-05
Application #
2130960
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Project Start
1991-07-01
Project End
1997-06-30
Budget Start
1995-07-01
Budget End
1997-06-30
Support Year
5
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Pediatrics
Type
Schools of Medicine
DUNS #
City
Houston
State
TX
Country
United States
Zip Code
77225
Steinwachs, E F; Amos, C; Johnston, D et al. (2000) Nonsyndromic cleft lip and palate is not associated with cancer or other birth defects. Am J Med Genet 90:17-24
Griffith, A J; Burgess, D L; Kohrman, D C et al. (1996) Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO. Genomics 34:299-303
Blanton, S H; Crowder, E; Malcolm, S et al. (1996) Exclusion of linkage between cleft lip with or without cleft palate and markers on chromosomes 4 and 6. Am J Hum Genet 58:239-41
Stein, J; Mulliken, J B; Stal, S et al. (1995) Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. Am J Hum Genet 57:257-72
Feng, H; Sassani, R; Bartlett, S P et al. (1994) Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate. Am J Hum Genet 55:932-6
Hecht, J T; Wang, Y; Connor, B et al. (1993) Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A. Am J Hum Genet 52:1230-3
Biddinger, A L; Hecht, J T; Milewicz, D M (1993) Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2). Hum Mol Genet 2:1323
Hecht, J T; Francomano, C A; Briggs, M D et al. (1993) Linkage of typical pseudoachondroplasia to chromosome 19. Genomics 18:661-6
Wang, Y; Sadler, L; Hecht, J T (1992) Polymorphic dinucleotide repeat in a cartilage matrix protein (CRTM) gene. Hum Mol Genet 1:780