HG00965/HG/NHGRI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1994	3
1995	7
1996	6
1997	6
2024	0

1

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.

Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley JD. Kobayashi H, et al. Blood. 1994 Nov 15;84(10):3473-82. Blood. 1994. PMID: 7949101 Free article. Clinical Trial.

2

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE. Basson CT, et al. Nat Genet. 1997 Jan;15(1):30-5. doi: 10.1038/ng0197-30. Nat Genet. 1997. PMID: 8988165

3

Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas.

Schoenberg Fejzo M, Ashar HR, Krauter KS, Powell WL, Rein MS, Weremowicz S, Yoon SJ, Kucherlapati RS, Chada K, Morton CC. Schoenberg Fejzo M, et al. Genes Chromosomes Cancer. 1996 Sep;17(1):1-6. doi: 10.1002/(SICI)1098-2264(199609)17:1<1::AID-GCC1>3.0.CO;2-0. Genes Chromosomes Cancer. 1996. PMID: 8889500

4

Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12.

Engle EC, Marondel I, Houtman WA, de Vries B, Loewenstein A, Lazar M, Ward DC, Kucherlapati R, Beggs AH. Engle EC, et al. Am J Hum Genet. 1995 Nov;57(5):1086-94. Am J Hum Genet. 1995. PMID: 7485159 Free PMC article.

5

Assignment of the human myogenic factors 5 and 6 (MYF5, MYF6) gene cluster to 12q21 by in situ hybridization and physical mapping of the locus between D12S350 and D12S106.

Cupelli L, Renault B, Leblanc-Straceski J, Banks A, Ward D, Kucherlapati RS, Krauter K. Cupelli L, et al. Cytogenet Cell Genet. 1996;72(2-3):250-1. doi: 10.1159/000134201. Cytogenet Cell Genet. 1996. PMID: 8978788 No abstract available.

6

A sequence-ready physical map of a region of 12q24.1.

Renault B, Hovnanian A, Bryce S, Chang JJ, Lau S, Sakuntabhai A, Monk S, Carter S, Ross CJ, Pang J, Twells R, Chamberlain S, Monaco AP, Strachan T, Kucherlapati R. Renault B, et al. Genomics. 1997 Oct 15;45(2):271-8. doi: 10.1006/geno.1997.4888. Genomics. 1997. PMID: 9344649

7

Physical mapping of a commonly deleted region, the site of a candidate tumor suppressor gene, at 12q22 in human male germ cell tumors.

Murty VV, Renault B, Falk CT, Bosl GJ, Kucherlapati R, Chaganti RS. Murty VV, et al. Genomics. 1996 Aug 1;35(3):562-70. doi: 10.1006/geno.1996.0398. Genomics. 1996. PMID: 8812492

8

QAV: querying entity-attribute-value metadata in a biomedical database.

Nadkarni PM. Nadkarni PM. Comput Methods Programs Biomed. 1997 Jun;53(2):93-103. doi: 10.1016/s0169-2607(97)01815-4. Comput Methods Programs Biomed. 1997. PMID: 9186046 Free article.

9

Identification of new translocation breakpoints at 12q13 in lipomas.

Merscher S, Marondel I, Pedeutour F, Gaudray P, Kucherlapati R, Turc-Carel C. Merscher S, et al. Genomics. 1997 Nov 15;46(1):70-7. doi: 10.1006/geno.1997.4993. Genomics. 1997. PMID: 9403060

10

Concept locator: a client-server application for retrieval of UMLS metathesaurus concepts through complex boolean query.

Nadkarni PM. Nadkarni PM. Comput Biomed Res. 1997 Aug;30(4):323-36. doi: 10.1006/cbmr.1997.1433. Comput Biomed Res. 1997. PMID: 9339325 Free article.

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