Vance GH - Search Results

1

Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implications.

Walsh LE, Vance GH, Weaver DD. Walsh LE, et al. Among authors: vance gh. Am J Med Genet. 2001 Jan 15;98(2):137-44. doi: 10.1002/1096-8628(20010115)98:2<137::aid-ajmg1022>3.0.co;2-5. Am J Med Genet. 2001. PMID: 11223849 Review.

2

Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia.

Palmer CG, Blouin JL, Bull MJ, Breitfeld P, Vance GH, Van Meter T, Weaver DD, Heerema NA, Colbern SG, Korenberg JR, et al. Palmer CG, et al. Among authors: vance gh. Am J Med Genet. 1995 Jul 17;57(4):527-36. doi: 10.1002/ajmg.1320570403. Am J Med Genet. 1995. PMID: 7573123

3

Cytogenetic findings of a child with transcobalamin II deficiency.

Vance GH, Moncino M, Heerema NA. Vance GH, et al. Am J Med Genet. 1993 Jul 1;46(6):615-9. doi: 10.1002/ajmg.1320460602. Am J Med Genet. 1993. PMID: 8362900

4

Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients.

Heerema NA, Maben KD, Bernstein J, Breitfeld PP, Neiman RS, Vance GH. Heerema NA, et al. Among authors: vance gh. Cancer Genet Cytogenet. 1996 Dec;92(2):111-5. doi: 10.1016/s0165-4608(96)00172-0. Cancer Genet Cytogenet. 1996. PMID: 8976366

5

Mild "duplication 6q syndrome": a case with partial trisomy (6)(q23.3q25.3).

Henegariu O, Heerema NA, Vance GH. Henegariu O, et al. Among authors: vance gh. Am J Med Genet. 1997 Feb 11;68(4):450-4. doi: 10.1002/(sici)1096-8628(19970211)68:4<450::aid-ajmg15>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9021020 Review.

6

Toward quality assurance for metaphase FISH: a multicenter experience.

Dewald GW, Stallard R, Bader PI, Chen K, Zenger-Hain J, Harris CJ, Higgins R, Hirsch B, Hsu WT, Johnson E, Kubic V, Kurczynski TW, Malone JM, McCorquodale DJ, Meilinger K, Meisner LF, Moore JW, Schwartz S, Siembieda S, Storto PD, Vance G, Van Tuinen P, Wiktor A, Yung JF. Dewald GW, et al. Am J Med Genet. 1996 Oct 28;65(3):190-6. doi: 10.1002/(SICI)1096-8628(19961028)65:3<190::AID-AJMG4>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 9240742

7

A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.

Henegariu O, Pescovitz OH, Vance GH, Verbrugge J, Heerema NA. Henegariu O, et al. Among authors: vance gh. Am J Med Genet. 1997 Sep 5;71(4):426-9. Am J Med Genet. 1997. PMID: 9286449

8

An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences.

Vance GH, Curtis CA, Heerema NA, Schwartz S, Palmer CG. Vance GH, et al. Am J Med Genet. 1997 Sep 5;71(4):436-42. doi: 10.1002/(sici)1096-8628(19970905)71:4<436::aid-ajmg13>3.0.co;2-h. Am J Med Genet. 1997. PMID: 9286452 Review.

9

Urorectal septum malformation sequence: report of thirteen additional cases and review of the literature.

Wheeler PG, Weaver DD, Obeime MO, Vance GH, Bull MJ, Escobar LF. Wheeler PG, et al. Among authors: vance gh. Am J Med Genet. 1997 Dec 31;73(4):456-62. Am J Med Genet. 1997. PMID: 9415474 Review.

10

Cytogenetics: a short review and update.

Vance GH. Vance GH. Cancer Invest. 1998;16(1):40-4. doi: 10.3109/07357909809039752. Cancer Invest. 1998. PMID: 9474250 Review. No abstract available.

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