Dobyns WB - Search Results

1

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.

2

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

3

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.

4

Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly.

Dobyns WB, Kirkpatrick JB, Hittner HM, Roberts RM, Kretzer FL. Dobyns WB, et al. Am J Med Genet. 1985 Sep;22(1):157-95. doi: 10.1002/ajmg.1320220118. Am J Med Genet. 1985. PMID: 3931474 Review.

5

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

6

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

7

Classical lissencephaly syndromes: does the face reflect the brain?

Allanson JE, Ledbetter DH, Dobyns WB. Allanson JE, et al. Among authors: dobyns wb. J Med Genet. 1998 Nov;35(11):920-3. doi: 10.1136/jmg.35.11.920. J Med Genet. 1998. PMID: 9832039 Free PMC article.

8

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.

Dobyns WB, Berry-Kravis E, Havernick NJ, Holden KR, Viskochil D. Dobyns WB, et al. Am J Med Genet. 1999 Oct 8;86(4):331-7. Am J Med Genet. 1999. PMID: 10494089 Review.

9

Familial lissencephaly with cleft palate and severe cerebellar hypoplasia.

Kerner B, Graham JM Jr, Golden JA, Pepkowitz SH, Dobyns WB. Kerner B, et al. Among authors: dobyns wb. Am J Med Genet. 1999 Dec 22;87(5):440-5. Am J Med Genet. 1999. PMID: 10594886

10

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.

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