Dobyns WB - Search Results

1

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.

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

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.

4

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.

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

Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction.

Batanian JR, Ledbetter SA, Wolff RK, Nakamura Y, White R, Dobyns WB, Ledbetter DH. Batanian JR, et al. Among authors: dobyns wb. Hum Genet. 1990 Oct;85(5):555-9. doi: 10.1007/BF00194237. Hum Genet. 1990. PMID: 2227942

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

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.

9

Familial pericentric and paracentric inversions of chromosome 1.

Johnson DD, Dobyns WB, Gordon H, Dewald GW. Johnson DD, et al. Among authors: dobyns wb. Hum Genet. 1988 Aug;79(4):315-20. doi: 10.1007/BF00282168. Hum Genet. 1988. PMID: 3410456

10

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

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