Demacio PC, Ray PN.
Alpha-catulin maps to the familial dysautonomia region on 9q31.
Genome. 2001 Dec;44(6):990-4.
PMID: 11768226
Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW.
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
Genomics. 2001 Nov;78(1-2):7-11.
PMID: 11707066
Osborne LR, Li M, Pober B, Chitayat D, Bodurtha J, Mandel A, Costa T, Grebe T, Cox S, Tsui LC, Scherer SW.
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.
Nat Genet. 2001 Nov;29(3):321-5.
PMID: 11685205
Dar P, Javed AA, Ben-Yishay M, Ferreira JC, Paterson AD, Gross SJ, Chitayat D, Morrow BE, Nitowsky HM.
Potential mapping of corneal dermoids to Xq24-qter.
J Med Genet. 2001 Oct;38(10):719-23. No abstract available.
PMID: 11594343
Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE.
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
Nat Genet. 2001 Oct;29(2):166-73.
PMID: 11586298
Wen XY, Stewart AK, Skaug J, Wei E, Tsui LC.
Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to chromosome 16 but is distinct from the lpd (lipid defect) locus.
Mamm Genome. 2001 Feb;12(2):129-32.
PMID: 11210182