Weksberg R - Search Results

1

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.

Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R, Leonard CO, Burton BK, Josephson KD, Laxová R, Aleck KA, Allanson JE, Guion-Almeida ML, Martin RA, Leichtman LG, Price RA, Opitz JM, Muenke M. Robin NH, et al. Among authors: weksberg r. Nat Genet. 1995 Dec;11(4):459-61. doi: 10.1038/ng1295-459. Nat Genet. 1995. PMID: 7493033

2

22q11 deletion syndrome in adults with schizophrenia.

Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. Bassett AS, et al. Among authors: weksberg r. Am J Med Genet. 1998 Jul 10;81(4):328-37. Am J Med Genet. 1998. PMID: 9674980 Free PMC article.

3

Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome.

Brzustowicz LM, Farrell S, Khan MB, Weksberg R. Brzustowicz LM, et al. Among authors: weksberg r. Am J Hum Genet. 1999 Sep;65(3):779-83. doi: 10.1086/302527. Am J Hum Genet. 1999. PMID: 10441586 Free PMC article.

4

Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.

Barr CL, Best L, Weksberg R. Barr CL, et al. Among authors: weksberg r. Am J Med Genet. 2001 Nov 22;104(2):120-6. doi: 10.1002/ajmg.1587. Am J Med Genet. 2001. PMID: 11746041

5

Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics.

Chow EW, Bassett AS, Weksberg R. Chow EW, et al. Among authors: weksberg r. Am J Med Genet. 1994 Jun 15;54(2):107-12. doi: 10.1002/ajmg.1320540205. Am J Med Genet. 1994. PMID: 8074160 Free PMC article.

6

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.

Weksberg R, Shen DR, Fei YL, Song QL, Squire J. Weksberg R, et al. Nat Genet. 1993 Oct;5(2):143-50. doi: 10.1038/ng1093-143. Nat Genet. 1993. PMID: 8252039

7

Glypicans: a growing trend.

Weksberg R, Squire JA, Templeton DM. Weksberg R, et al. Nat Genet. 1996 Mar;12(3):225-7. doi: 10.1038/ng0396-225. Nat Genet. 1996. PMID: 8589707 No abstract available.

8

Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.

Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R. Terespolsky D, et al. Among authors: weksberg r. Am J Med Genet. 1995 Nov 20;59(3):329-33. doi: 10.1002/ajmg.1320590310. Am J Med Genet. 1995. PMID: 8599356

9

Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia.

Bernard LE, Chitayat D, Weksberg R, Van Allen MI, Langlois S. Bernard LE, et al. Among authors: weksberg r. J Med Genet. 1996 May;33(5):432-4. doi: 10.1136/jmg.33.5.432. J Med Genet. 1996. PMID: 8733060 Free PMC article.

10

FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.

Teshima I, Chadwick D, Chitayat D, Kobayashi J, Ray P, Shuman C, Siegel-Bartelt J, Strasberg P, Weksberg R. Teshima I, et al. Among authors: weksberg r. Am J Med Genet. 1996 Mar 29;62(3):217-23. doi: 10.1002/(sici)1096-8628(19960329)62:3<216::aid-ajmg3>3.3.co;2-0. Am J Med Genet. 1996. PMID: 8882776

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