Dobyns WB - Search Results

1

Antibodies to ACTH in opsoclonus-myoclonus.

Pranzatelli MR, Kao PC, Tate ED, Chaves E, Chez M, Dobyns WB, Kang H, Rothner DA. Pranzatelli MR, et al. Among authors: dobyns wb. Neuropediatrics. 1993 Jun;24(3):131-3. doi: 10.1055/s-2008-1071529. Neuropediatrics. 1993. PMID: 8395029 Review.

2

Lissencephaly and other malformations of cortical development: 1995 update.

Dobyns WB, Truwit CL. Dobyns WB, et al. Neuropediatrics. 1995 Jun;26(3):132-47. doi: 10.1055/s-2007-979744. Neuropediatrics. 1995. PMID: 7477752 Review.

3

Cobblestone lissencephaly with normal eyes and muscle.

Dobyns WB, Patton MA, Stratton RF, Mastrobattista JM, Blanton SH, Northrup H. Dobyns WB, et al. Neuropediatrics. 1996 Apr;27(2):70-5. doi: 10.1055/s-2007-973752. Neuropediatrics. 1996. PMID: 8737821

4

Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.

Ross ME, Swanson K, Dobyns WB. Ross ME, et al. Among authors: dobyns wb. Neuropediatrics. 2001 Oct;32(5):256-63. doi: 10.1055/s-2001-19120. Neuropediatrics. 2001. PMID: 11748497

5

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.

Northrup H, Kwiatkowski DJ, Roach ES, Dobyns WB, Lewis RA, Herman GE, Rodriguez E Jr, Daiger SP, Blanton SH. Northrup H, et al. Among authors: dobyns wb. Am J Hum Genet. 1992 Oct;51(4):709-20. Am J Hum Genet. 1992. PMID: 1415216 Free PMC article.

6

Causal heterogeneity in isolated lissencephaly.

Dobyns WB, Elias ER, Newlin AC, Pagon RA, Ledbetter DH. Dobyns WB, et al. Neurology. 1992 Jul;42(7):1375-88. doi: 10.1212/wnl.42.7.1375. Neurology. 1992. PMID: 1620349

7

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

8

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

9

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.

Greenberg F, Stratton RF, Lockhart LH, Elder FF, Dobyns WB, Ledbetter DH. Greenberg F, et al. Among authors: dobyns wb. Am J Med Genet. 1986 Apr;23(4):853-9. doi: 10.1002/ajmg.1320230402. Am J Med Genet. 1986. PMID: 3963054

10

Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly.

Dobyns WB, Stratton RF, Greenberg F. Dobyns WB, et al. Am J Med Genet. 1984 Jul;18(3):509-26. doi: 10.1002/ajmg.1320180320. Am J Med Genet. 1984. PMID: 6476009

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

442 results

Search Page

Filters