Flannery DB - Search Results

1

Packed red cell transfusion does not compromise chromosome analysis in newborns.

Kulharya AS, Salbert BA, Norris KN, Cook L, Larrison PJ, Flannery DB. Kulharya AS, et al. Among authors: flannery db. Genet Med. 2001 Jul-Aug;3(4):314-7. doi: 10.1097/00125817-200107000-00008. Genet Med. 2001. PMID: 11478533 Free article.

2

Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.

Kulharya AS, Lovell CM, Flannery DB. Kulharya AS, et al. Among authors: flannery db. Am J Med Genet. 2002 Dec 15;113(4):367-70. doi: 10.1002/ajmg.b.10801. Am J Med Genet. 2002. PMID: 12457409

3

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.

Kulharya AS, Flannery DB, Norris K, Lovell C, Levy B, Velagaleti GV. Kulharya AS, et al. Among authors: flannery db. Am J Med Genet A. 2008 Sep 1;146A(17):2234-41. doi: 10.1002/ajmg.a.32397. Am J Med Genet A. 2008. PMID: 18666229

4

Complete monosomy 21 confirmed by FISH and array-CGH.

Kulharya AS, Tonk VS, Lovell C, Flannery DB. Kulharya AS, et al. Among authors: flannery db. Am J Med Genet A. 2012 Apr;158A(4):935-7. doi: 10.1002/ajmg.a.35251. Epub 2012 Mar 9. Am J Med Genet A. 2012. PMID: 22407893 No abstract available.

5

Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker.

Kulharya AS, Garcia-Heras J, Radtke HB, Norris KS, Keppen LD, Flannery DB. Kulharya AS, et al. Among authors: flannery db. Clin Genet. 1998 Nov;54(5):421-5. doi: 10.1111/j.1399-0004.1998.tb03757.x. Clin Genet. 1998. PMID: 9842996

6

Ring chromosome 5.

Flannery DB, Rogers WG, Byrd JR. Flannery DB, et al. Clin Genet. 1988 Jul;34(1):74-8. doi: 10.1111/j.1399-0004.1988.tb02619.x. Clin Genet. 1988. PMID: 3409543

7

Depiction of gene-environment relationships in online medical recommendations.

Cheng Y, Condit C, Flannery D. Cheng Y, et al. Genet Med. 2008 Jun;10(6):450-6. doi: 10.1097/gim.0b013e31817701a8. Genet Med. 2008. PMID: 18496221

8

Frontofacionasal dysplasia.

White EW, Figueroa R, Flannery DB. White EW, et al. Among authors: flannery db. Am J Med Genet. 1991 Sep 1;40(3):338-40. doi: 10.1002/ajmg.1320400318. Am J Med Genet. 1991. PMID: 1951440 No abstract available.

9

Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism.

Flannery DB. Flannery DB. Am J Med Genet. 1990 Jan;35(1):18-21. doi: 10.1002/ajmg.1320350105. Am J Med Genet. 1990. PMID: 2405667 Review. No abstract available.

10

An apparent de novo terminal deletion of chromosome 2 (pter----p24:).

Francis GL, Flannery DB, Byrd JR, Fisher ST. Francis GL, et al. Among authors: flannery db. J Med Genet. 1990 Feb;27(2):137-8. doi: 10.1136/jmg.27.2.137. J Med Genet. 1990. PMID: 2319584 Free PMC article. No abstract available.

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