Dobyns WB - Search Results

1

Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.

Dobyns WB, Dewald GW, Carlson RO, Mair DD, Michels VV. Dobyns WB, et al. Am J Med Genet. 1985 Sep;22(1):125-34. doi: 10.1002/ajmg.1320220114. Am J Med Genet. 1985. PMID: 3901750 Review.

2

Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly.

Ledbetter SA, Kuwano A, Dobyns WB, Ledbetter DH. Ledbetter SA, et al. Among authors: dobyns wb. Am J Hum Genet. 1992 Jan;50(1):182-9. Am J Hum Genet. 1992. PMID: 1346078 Free PMC article.

3

Clinical and molecular diagnosis of Miller-Dieker syndrome.

Dobyns WB, Curry CJ, Hoyme HE, Turlington L, Ledbetter DH. Dobyns WB, et al. Am J Hum Genet. 1991 Mar;48(3):584-94. Am J Hum Genet. 1991. PMID: 1671808 Free PMC article.

4

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Greenberg F, Guzzetta V, Montes de Oca-Luna R, Magenis RE, Smith AC, Richter SF, Kondo I, Dobyns WB, Patel PI, Lupski JR. Greenberg F, et al. Among authors: dobyns wb. Am J Hum Genet. 1991 Dec;49(6):1207-18. Am J Hum Genet. 1991. PMID: 1746552 Free PMC article.

5

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.

Kuwano A, Ledbetter SA, Dobyns WB, Emanuel BS, Ledbetter DH. Kuwano A, et al. Among authors: dobyns wb. Am J Hum Genet. 1991 Oct;49(4):707-14. Am J Hum Genet. 1991. PMID: 1897521 Free PMC article.

6

Diagnostic criteria for Walker-Warburg syndrome.

Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M, et al. Dobyns WB, et al. Am J Med Genet. 1989 Feb;32(2):195-210. doi: 10.1002/ajmg.1320320213. Am J Med Genet. 1989. PMID: 2494887

7

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.

vanTuinen P, Dobyns WB, Rich DC, Summers KM, Robinson TJ, Nakamura Y, Ledbetter DH. vanTuinen P, et al. Among authors: dobyns wb. Am J Hum Genet. 1988 Nov;43(5):587-96. Am J Hum Genet. 1988. PMID: 3189330 Free PMC article.

8

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.

Kelley RI, Datta NS, Dobyns WB, Hajra AK, Moser AB, Noetzel MJ, Zackai EH, Moser HW. Kelley RI, et al. Among authors: dobyns wb. Am J Med Genet. 1986 Apr;23(4):869-901. doi: 10.1002/ajmg.1320230404. Am J Med Genet. 1986. PMID: 3515938 Review.

9

Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.

Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM, et al. Stratton RF, et al. Among authors: dobyns wb. Am J Med Genet. 1986 Jul;24(3):421-32. doi: 10.1002/ajmg.1320240305. Am J Med Genet. 1986. PMID: 3728561

10

Further comments on the lissencephaly syndromes.

Dobyns WB, Gilbert EF, Opitz JM. Dobyns WB, et al. Am J Med Genet. 1985 Sep;22(1):197-211. doi: 10.1002/ajmg.1320220119. Am J Med Genet. 1985. PMID: 3901751 Review.

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