McDermid H - Search Results

1

The role of cytologic NOR variants in the etiology of trisomy 21.

Spinner NB, Eunpu DL, Schmickel RD, Zackai EH, McEldrew D, Bunin GR, McDermid H, Emanuel BS. Spinner NB, et al. Among authors: mcdermid h. Am J Hum Genet. 1989 May;44(5):631-8. Am J Hum Genet. 1989. PMID: 2523191 Free PMC article. Review.

2

Molecular studies of DiGeorge syndrome.

Fibison WJ, Budarf M, McDermid H, Greenberg F, Emanuel BS. Fibison WJ, et al. Among authors: mcdermid h. Am J Hum Genet. 1990 May;46(5):888-95. Am J Hum Genet. 1990. PMID: 2339689 Free PMC article.

3

Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.

Budarf ML, McDermid HE, Sellinger B, Emanuel BS. Budarf ML, et al. Among authors: mcdermid he. Genomics. 1991 Aug;10(4):996-1002. doi: 10.1016/0888-7543(91)90190-p. Genomics. 1991. PMID: 1680800

4

Toward a long-range map of human chromosomal band 22q11.

McDermid HE, Budarf ML, Emanuel BS. McDermid HE, et al. Genomics. 1989 Jul;5(1):1-8. doi: 10.1016/0888-7543(89)90079-7. Genomics. 1989. PMID: 2788606

5

Molecular characterization of the marker chromosome associated with cat eye syndrome.

Mears AJ, Duncan AM, Budarf ML, Emanuel BS, Sellinger B, Siegel-Bartelt J, Greenberg CR, McDermid HE. Mears AJ, et al. Among authors: mcdermid he. Am J Hum Genet. 1994 Jul;55(1):134-42. Am J Hum Genet. 1994. PMID: 7912885 Free PMC article.

6

Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.

Holmes SE, Riazi MA, Gong W, McDermid HE, Sellinger BT, Hua A, Chen F, Wang Z, Zhang G, Roe B, Gonzalez I, McDonald-McGinn DM, Zackai E, Emanuel BS, Budarf ML. Holmes SE, et al. Among authors: mcdermid he. Hum Mol Genet. 1997 Mar;6(3):357-67. doi: 10.1093/hmg/6.3.357. Hum Mol Genet. 1997. PMID: 9147638

7

Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panel.

Budarf ML, Eckman B, Michaud D, McDonald T, Gavigan S, Buetow KH, Tatsumura Y, Liu Z, Hilliard C, Driscoll D, Goldmuntz E, Meese E, Zwarthoff EC, Williams S, McDermid H, Dumanski JP, Biegel J, Bell CJ, Emanuel BS. Budarf ML, et al. Among authors: mcdermid h. Genomics. 1996 Jul 15;35(2):275-88. doi: 10.1006/geno.1996.0358. Genomics. 1996. PMID: 8661140 Free article.

8

Mapping of the human lambda immunoglobulin variable gene subgroup 1.

McDermid HE, Emanuel BS. McDermid HE, et al. Immunogenetics. 1994;40(3):177-83. doi: 10.1007/BF00167077. Immunogenetics. 1994. PMID: 8039825

9

Long-range restriction map of human chromosome 22q11-22q12 between the lambda immunoglobulin locus and the Ewing sarcoma breakpoint.

McDermid HE, Budarf ML, Emanuel BS. McDermid HE, et al. Genomics. 1993 Nov;18(2):308-18. doi: 10.1006/geno.1993.1470. Genomics. 1993. PMID: 7507075

10

Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints.

McTaggart KE, Budarf ML, Driscoll DA, Emanuel BS, Ferreira P, McDermid HE. McTaggart KE, et al. Among authors: mcdermid he. Cytogenet Cell Genet. 1998;81(3-4):222-8. doi: 10.1159/000015035. Cytogenet Cell Genet. 1998. PMID: 9730608

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