Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Dasouki, M; Jurecic, V; Phillips 3rd, J A et al. (1997) DiGeorge anomaly and chromosome 10p deletions: one or two loci? Am J Med Genet 73:72-5
Williams, J B; Rexer, B; Sirripurapu, S et al. (1997) The human HNP36 gene is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia, type 1 (MEN I) syndrome. Genomics 42:325-30
Raskin, S; Philips 3rd, J A; Krishnamani, M R et al. (1997) Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study. Hum Biol 69:75-88
Repaske, D R; Medlej, R; Gultekin, E K et al. (1997) Heterogeneity in clinical manifestation of autosomal dominant neurohypophyseal diabetes insipidus caused by a mutation encoding Ala-1-->Val in the signal peptide of the arginine vasopressin/neurophysin II/copeptin precursor. J Clin Endocrinol Metab 82:51-6
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Spearman, P; Ratner, L (1996) Human immunodeficiency virus type 1 capsid formation in reticulocyte lysates. J Virol 70:8187-94
Martincic, D; Whitlock, J A (1996) Improved detection of p53 point mutations by dideoxyfingerprinting (ddF). Oncogene 13:2039-44
Cogan, J D; Ramel, B; Lehto, M et al. (1995) A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study. J Clin Endocrinol Metab 80:3591-5
Summar, M L; Dasouki, M J; Schofield, P J et al. (1995) Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35. Cytogenet Cell Genet 71:266-7
Campbell 3rd, P W; Phillips 3rd, J A; Heidecker, G J et al. (1995) Detection of Pseudomonas (Burkholderia) cepacia using PCR. Pediatr Pulmonol 20:44-9

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