Syndrome of imperforate oropharynx with costovertebral and auricular anomaliesFLANNERY, D. B.American journal of medical genetics. 1989, Vol 32, Num 2, pp 189-191, issn 0148-7299Article

Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicismFLANNERY, D. B.American journal of medical genetics. 1990, Vol 35, Num 1, pp 18-21, issn 0148-7299Article

Tests appropriate for the prenatal diagnosis of ataxia telangiectasiaSCHWARTZ, S; FLANNERY, D. B; COHEN, M. M et al.Prenatal diagnosis. 1985, Vol 5, Num 1, pp 9-14, issn 0197-3851Article

Craniofrontonasal dysplasia: clinical and genetic analysisSAX, C. M; FLANNERY, D. B.Clinical genetics. 1986, Vol 29, Num 6, pp 508-515, issn 0009-9163Article

Sinus venosus atrial septal defect and pacemaker requirement in a familyARENSMAN, F. W; BOINEAU, J. P; BALFOUR, I. C et al.The American journal of cardiology. 1986, Vol 57, Num 4, pp 368-369, issn 0002-9149Article

Amino acids in amniotic fluid in the second trimester of gestationMESAVAGE, W. C; SUCHY, S. F; WEINER, D. L et al.Pediatric research. 1985, Vol 19, Num 10, pp 1021-1024, issn 0031-3998Article

Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited markerKULHARYA, A. S; GARCIA-HERAS, J; RADTKE, H. B et al.Clinical genetics. 1998, Vol 54, Num 5, pp 421-425, issn 0009-9163Article

The Schinzel-Giedion syndromeAL-GAZALI, L. I; FARNDON, P; BURN, J et al.Journal of medical genetics. 1990, Vol 27, Num 1, pp 42-47, issn 0022-2593, 6 p.Article

Transient infantile osteopetrosisMONAGHAN, B. A; KAPLAN, F. S; AUGUST, C. S et al.The Journal of pediatrics. 1991, Vol 118, Num 2, pp 252-256, issn 0022-3476Article

An apparent de novo terminal deletion of chromosome 2 (pter→p24:)FRANCIS, G. L; FLANNERY, D. B; BYRD, J. R et al.Journal of medical genetics. 1990, Vol 27, Num 2, pp 137-138, issn 0022-2593, 2 p.Article

3-M syndrome. Comment. ReplyFLANNERY, D. B; HENNEKAM, R. C. M; SPRANGER, J et al.American journal of medical genetics. 1989, Vol 32, Num 2, pp 252-254, issn 0148-7299Article

Verification of the fetal valproate syndrome phenotypeARDINGER, H. H; ATKIN, J. F; MAJEWSKI, F et al.American journal of medical genetics. 1988, Vol 29, Num 1, pp 171-185, issn 0148-7299Article

Hypertrichosis cubitiFLANNERY, D. B; FINK, S. M; FRANCIS, G et al.American journal of medical genetics. 1989, Vol 32, Num 4, pp 482-483, issn 0148-7299Article

Ring chromosome 5FLANNERY, D. B; ROGERS, W. G; BYRD, J. R et al.Clinical genetics. 1988, Vol 34, Num 1, pp 74-78, issn 0009-9163Article

Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndromeSCHWARTZ, C. E; JOHNSON, J. P; FLANNERY, D. B et al.American journal of human genetics. 1988, Vol 43, Num 5, pp 597-604, issn 0002-9297Article

Johanson-Blizzard syndrome and hypopituitarismKRISTJANSSON, K; HOFFMAN, W. H; FLANNERY, D. B et al.The Journal of pediatrics. 1988, Vol 113, Num 5, pp 851-853, issn 0022-3476Article