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Items: 45

1.

Challenges and opportunities for effective delivery of clinical genetic services in the U.S. healthcare system.

Flannery DB.

Curr Opin Pediatr. 2018 Dec;30(6):740-745. doi: 10.1097/MOP.0000000000000693.

PMID:
30199404
2.

Complete monosomy 21 confirmed by FISH and array-CGH.

Kulharya AS, Tonk VS, Lovell C, Flannery DB.

Am J Med Genet A. 2012 Apr;158A(4):935-7. doi: 10.1002/ajmg.a.35251. Epub 2012 Mar 9. No abstract available.

PMID:
22407893
3.

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.

Stankiewicz P, Kulkarni S, Dharmadhikari AV, Sampath S, Bhatt SS, Shaikh TH, Xia Z, Pursley AN, Cooper ML, Shinawi M, Paciorkowski AR, Grange DK, Noetzel MJ, Saunders S, Simons P, Summar M, Lee B, Scaglia F, Fellmann F, Martinet D, Beckmann JS, Asamoah A, Platky K, Sparks S, Martin AS, Madan-Khetarpal S, Hoover J, Medne L, Bonnemann CG, Moeschler JB, Vallee SE, Parikh S, Irwin P, Dalzell VP, Smith WE, Banks VC, Flannery DB, Lovell CM, Bellus GA, Golden-Grant K, Gorski JL, Kussmann JL, McGregor TL, Hamid R, Pfotenhauer J, Ballif BC, Shaw CA, Kang SH, Bacino CA, Patel A, Rosenfeld JA, Cheung SW, Shaffer LG.

Hum Mutat. 2012 Jan;33(1):165-79. doi: 10.1002/humu.21614. Epub 2011 Nov 2.

4.

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.

Am J Med Genet A. 2008 Sep 1;146A(17):2234-41. doi: 10.1002/ajmg.a.32397.

PMID:
18666229
5.

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

Johnston JJ, Olivos-Glander I, Killoran C, Elson E, Turner JT, Peters KF, Abbott MH, Aughton DJ, Aylsworth AS, Bamshad MJ, Booth C, Curry CJ, David A, Dinulos MB, Flannery DB, Fox MA, Graham JM, Grange DK, Guttmacher AE, Hannibal MC, Henn W, Hennekam RC, Holmes LB, Hoyme HE, Leppig KA, Lin AE, Macleod P, Manchester DK, Marcelis C, Mazzanti L, McCann E, McDonald MT, Mendelsohn NJ, Moeschler JB, Moghaddam B, Neri G, Newbury-Ecob R, Pagon RA, Phillips JA, Sadler LS, Stoler JM, Tilstra D, Walsh Vockley CM, Zackai EH, Zadeh TM, Brueton L, Black GC, Biesecker LG.

Am J Hum Genet. 2005 Apr;76(4):609-22. Epub 2005 Feb 28.

7.

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

Kulharya AS, Salbert BA, Norris KN, Cook L, Larrison PJ, Flannery DB.

Genet Med. 2001 Jul-Aug;3(4):314-7.

PMID:
11478533
8.

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.

Clin Genet. 1998 Nov;54(5):421-5.

PMID:
9842996
9.

Frontofacionasal dysplasia.

White EW, Figueroa R, Flannery DB.

Am J Med Genet. 1991 Sep 1;40(3):338-40. No abstract available.

PMID:
1951440
10.

Transient infantile osteopetrosis.

Monaghan BA, Kaplan FS, August CS, Fallon MD, Flannery DB.

J Pediatr. 1991 Feb;118(2):252-6. No abstract available.

PMID:
1993956
11.

Facial dysmorphologic and skeletal cephalometric findings associated with conotruncal cardiac anomalies. off.

Bell RA, Arensman FW, Flannery DB, Ussery TW, Moss RB.

Pediatr Dent. 1990 May-Jun;12(3):152-6.

PMID:
2077489
12.

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

Francis GL, Flannery DB, Byrd JR, Fisher ST.

J Med Genet. 1990 Feb;27(2):137-8. No abstract available.

13.

The Schinzel-Giedion syndrome.

al-Gazali LI, Farndon P, Burn J, Flannery DB, Davison C, Mueller RF.

J Med Genet. 1990 Jan;27(1):42-7. Review. No abstract available.

14.

Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism.

Flannery DB.

Am J Med Genet. 1990 Jan;35(1):18-21. Review. No abstract available.

PMID:
2405667
15.

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Thomas IT, Frias JL, Cantu ES, Lafer CZ, Flannery DB, Graham JG Jr.

Am J Hum Genet. 1989 Aug;45(2):193-205. Review.

16.

Hypertrichosis cubiti.

Flannery DB, Fink SM, Francis G, Gilman PA.

Am J Med Genet. 1989 Apr;32(4):482-3.

PMID:
2773989
17.

3-M syndrome.

Flannery DB.

Am J Med Genet. 1989 Feb;32(2):252-4. No abstract available.

PMID:
2929663
18.

Syndrome of imperforate oropharynx with costovertebral and auricular anomalies.

Flannery DB.

Am J Med Genet. 1989 Feb;32(2):189-91.

PMID:
2929659
19.

Johanson-Blizzard syndrome and hypopituitarism.

Kristjansson K, Hoffman WH, Flannery DB, Cohen MJ.

J Pediatr. 1988 Nov;113(5):851-3. No abstract available.

PMID:
3183841
20.

Joubert syndrome: early diagnosis by recognition of the behavioral phenotype and confirmation by cranial sonography.

Edwards BO Jr, Fischer AQ, Flannery DB.

J Child Neurol. 1988 Oct;3(4):247-9.

PMID:
3058780
21.

Nondisjunction in Down syndrome.

Flannery DB.

Am J Med Genet. 1988 Sep;31(1):181-2. No abstract available.

PMID:
2975924
22.

Ring chromosome 5.

Flannery DB, Rogers WG, Byrd JR.

Clin Genet. 1988 Jul;34(1):74-8.

PMID:
3409543
23.

Verification of the fetal valproate syndrome phenotype.

Ardinger HH, Atkin JF, Blackston RD, Elsas LJ, Clarren SK, Livingstone S, Flannery DB, Pellock JM, Harrod MJ, Lammer EJ, et al.

Am J Med Genet. 1988 Jan;29(1):171-85. Review.

PMID:
3125743
24.

The possible role of homeotic genes in the causation of malformations in monozygotic twins.

Flannery DB.

Acta Genet Med Gemellol (Roma). 1987;36(3):433-6.

PMID:
2897751
25.

Association of low blood manganese concentrations with epilepsy.

Carl GF, Keen CL, Gallagher BB, Clegg MS, Littleton WH, Flannery DB, Hurley LS.

Neurology. 1986 Dec;36(12):1584-7.

PMID:
3785672
26.

Craniofrontonasal dysplasia: clinical and genetic analysis.

Sax CM, Flannery DB.

Clin Genet. 1986 Jun;29(6):508-15.

PMID:
3742856
27.

Neural tube defects in trisomy 18.

Flannery DB, Kahler SG.

Prenat Diagn. 1986 Mar-Apr;6(2):97-9.

PMID:
3703824
28.

Sinus venosus atrial septal defect and pacemaker requirement in a family.

Arensman FW, Boineau JP, Balfour IC, Flannery DB, Moore HV.

Am J Cardiol. 1986 Feb 1;57(4):368-9. No abstract available.

PMID:
3946240
29.

Nucleolar organizer region variants as a risk factor for Down syndrome.

Jackson-Cook CK, Flannery DB, Corey LA, Nance WE, Brown JA.

Am J Hum Genet. 1985 Nov;37(6):1049-61.

30.

Amino acids in amniotic fluid in the second trimester of gestation.

Mesavage WC, Suchy SF, Weiner DL, Nance CS, Flannery DB, Wolf B.

Pediatr Res. 1985 Oct;19(10):1021-4.

PMID:
4058974
31.

Does isotretinoin cause limb reduction defects?

Lammer EJ, Flannery DB, Barr M.

Lancet. 1985 Aug 10;2(8450):328. No abstract available.

PMID:
2862487
32.

Prenatal testing and twinning.

Flannery DB, Holzman GB.

Clin Genet. 1985 Aug;28(2):180-2. No abstract available.

PMID:
4042404
33.

Dermatoglyphics in Börjeson-Forssman-Lehmann syndrome.

Flannery DB, Piussan C, Wright LE.

Am J Med Genet. 1985 Jun;21(2):401-4. No abstract available.

PMID:
4014320
34.

Tests appropriate for the prenatal diagnosis of ataxia telangiectasia.

Schwartz S, Flannery DB, Cohen MM.

Prenat Diagn. 1985 Jan-Feb;5(1):9-14.

PMID:
2579376
35.

Antenatally detected Klinefelter's syndrome in twins.

Flannery DB, Brown JA, Redwine FO, Winter P, Nance WE.

Acta Genet Med Gemellol (Roma). 1984;33(1):51-6.

PMID:
6741419
36.

Short rib-polydactyly syndrome type II (Majewski syndrome): a case report.

McCormac RM, Flannery DB, Nakoneczna I, Kodroff MB.

Pediatr Pathol. 1984;2(4):457-67.

PMID:
6535999
37.

Dietary management of phenylketonuria from birth using a phenylalanine-free product.

Flannery DB, Hitchcock E, Mamunes P.

J Pediatr. 1983 Aug;103(2):247-9. No abstract available.

PMID:
6875718
38.

Nonketotic hyperglycinemia in two retarded adults: a mild form of infantile nonketotic hyperglycinemia.

Flannery DB, Pellock J, Bousounis D, Hunt P, Nance C, Wolf B.

Neurology. 1983 Aug;33(8):1064-6.

PMID:
6683804
39.

Glycine/serine ratios in amniotic fluid: an unreliable indicator for the prenatal diagnosis of nonketotic hyperglycinemia.

Mesavage C, Nance CS, Flannery DB, Weiner DL, Suchy SF, Wolf B.

Clin Genet. 1983 May;23(5):354-8. No abstract available.

PMID:
6406113
40.

Cheirolumbar dysostosis: a phenotype of pseudohypoparathyroidism.

Halloran SL, Flannery DB, Kodroff MB, Santora AC 2nd, Wolf B.

Skeletal Radiol. 1983;10(3):161-4.

PMID:
6635689
41.

Current status of hyperammonemic syndromes.

Flannery DB, Hsia YE, Wolf B.

Hepatology. 1982 Jul-Aug;2(4):495-506. Review. No abstract available.

PMID:
7047351
42.

Pseudomonas sacroiliac osteomyelitis: diagnosis by gallium citrate Ga 67 scan.

Pope TL, Teague WG, Kossack R, Bray ST, Flannery DB.

Am J Dis Child. 1982 Jul;136(7):649-50. No abstract available.

PMID:
6211972
43.

Follow-up of a survivor of intrauterine lightning exposure.

Flannery DB, Wiles H.

Am J Obstet Gynecol. 1982 Jan 15;142(2):238-9. No abstract available.

PMID:
7055188
44.

Parent's knowledge about acetaminophen.

Flannery DB.

J Pediatr. 1981 May;98(5):851. No abstract available.

PMID:
7229776
45.

Simultaneous occurrence of extrahepatic biliary atresia and fetal alcohol syndrome.

Newman SL, Flannery DB, Caplan DB.

Am J Dis Child. 1979 Jan;133(1):101. No abstract available.

PMID:
760506

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