Hall B - Search Results

1

Personal journeys to and in human genetics and dysmorphology.

Schwartz CE, Aylsworth AS, Allanson J, Battaglia A, Carey JC, Curry CJ, Davies KE, Eichler EE, Graham JM Jr, Hall B, Hall JG, Holmes LB, Hoyme HE, Hunter A, Innis J, Johnson J, Keppler-Noreuil KM, Leroy JG, Moore C, Nelson DL, Neri G, Opitz JM, Picketts D, Raymond FL, Shalev SA, Stevenson RE, Stumpel CTRM, Sutherland G, Viskochil DH, Weaver DD, Zackai EH. Schwartz CE, et al. Among authors: hall jg, hall b. Am J Med Genet A. 2024 Jun;194(6):e63514. doi: 10.1002/ajmg.a.63514. Epub 2024 Feb 8. Am J Med Genet A. 2024. PMID: 38329159

2

Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1.

Verga V, Hall BK, Wang SR, Johnson S, Higgins JV, Glover TW. Verga V, et al. Among authors: hall bk. Am J Hum Genet. 1991 Jun;48(6):1133-8. Am J Hum Genet. 1991. PMID: 2035533 Free PMC article.

3

Isolation of a partial candidate gene for Menkes disease by positional cloning.

Mercer JF, Livingston J, Hall B, Paynter JA, Begy C, Chandrasekharappa S, Lockhart P, Grimes A, Bhave M, Siemieniak D, et al. Mercer JF, et al. Among authors: hall b. Nat Genet. 1993 Jan;3(1):20-5. doi: 10.1038/ng0193-20. Nat Genet. 1993. PMID: 8490647

4

Ten base pair duplication in exon 38 of the NF1 gene.

Legius E, Hall BK, Wallace MR, Collins FS, Glover TW. Legius E, et al. Among authors: hall bk. Hum Mol Genet. 1994 May;3(5):829-30. doi: 10.1093/hmg/3.5.829. Hum Mol Genet. 1994. PMID: 8081372 No abstract available.

5

FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites.

Wilke CM, Hall BK, Hoge A, Paradee W, Smith DI, Glover TW. Wilke CM, et al. Among authors: hall bk. Hum Mol Genet. 1996 Feb;5(2):187-95. doi: 10.1093/hmg/5.2.187. Hum Mol Genet. 1996. PMID: 8824874

6

Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragments.

Erickson RP, Glover TW, Hall BK, Witt M. Erickson RP, et al. Among authors: hall bk. Ann Hum Genet. 1991 Jul;55(3):199-211. doi: 10.1111/j.1469-1809.1991.tb00414.x. Ann Hum Genet. 1991. PMID: 1763884 Free article.

7

Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma.

Wilke CM, Guo SW, Hall BK, Boldog F, Gemmill RM, Chandrasekharappa SC, Barcroft CL, Drabkin HA, Glover TW. Wilke CM, et al. Among authors: hall bk. Genomics. 1994 Jul 15;22(2):319-26. doi: 10.1006/geno.1994.1390. Genomics. 1994. PMID: 7806217 Free article.

8

NF1-related locus on chromosome 15.

Legius E, Marchuk DA, Hall BK, Andersen LB, Wallace MR, Collins FS, Glover TW. Legius E, et al. Among authors: hall bk. Genomics. 1992 Aug;13(4):1316-8. doi: 10.1016/0888-7543(92)90055-w. Genomics. 1992. PMID: 1505963 Free article.

9

Severe insulin resistance and diabetes mellitus in mandibuloacral dysplasia.

Freidenberg GR, Cutler DL, Jones MC, Hall B, Mier RJ, Culler F, Jones KL, Lozzio C, Kaufmann S. Freidenberg GR, et al. Among authors: hall b. Am J Dis Child. 1992 Jan;146(1):93-9. doi: 10.1001/archpedi.1992.02160130095028. Am J Dis Child. 1992. PMID: 1736653

10

TP53 mutations are frequent in malignant NF1 tumors.

Legius E, Dierick H, Wu R, Hall BK, Marynen P, Cassiman JJ, Glover TW. Legius E, et al. Among authors: hall bk. Genes Chromosomes Cancer. 1994 Aug;10(4):250-5. doi: 10.1002/gcc.2870100405. Genes Chromosomes Cancer. 1994. PMID: 7522538

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