Weksberg R - Search Results

1

Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.

Nakabayashi K, Fernandez BA, Teshima I, Shuman C, Proud VK, Curry CJ, Chitayat D, Grebe T, Ming J, Oshimura M, Meguro M, Mitsuya K, Deb-Rinker P, Herbrick JA, Weksberg R, Scherer SW. Nakabayashi K, et al. Among authors: weksberg r. Genomics. 2002 Feb;79(2):186-96. doi: 10.1006/geno.2002.6695. Genomics. 2002. PMID: 11829489

2

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.

Weksberg R, Glaves M, Teshima I, Waziri M, Patil S, Williams BR. Weksberg R, et al. Genomics. 1990 Dec;8(4):693-8. doi: 10.1016/0888-7543(90)90256-t. Genomics. 1990. PMID: 2276740

3

Variant translocations of chromosome 22 in Ewing's sarcoma.

Squire J, Zielenska M, Thorner P, Tennyson S, Weitzman S, Pai KM, Yeger H, Ng YK, Weksberg R. Squire J, et al. Among authors: weksberg r. Genes Chromosomes Cancer. 1993 Nov;8(3):190-4. doi: 10.1002/gcc.2870080309. Genes Chromosomes Cancer. 1993. PMID: 7509628

4

Wilms tumor in a patient with Prader-Willi syndrome.

Coppes MJ, Sohl H, Teshima IE, Mutirangura A, Ledbetter DH, Weksberg R. Coppes MJ, et al. Among authors: weksberg r. J Pediatr. 1993 May;122(5 Pt 1):730-3. doi: 10.1016/s0022-3476(06)80015-6. J Pediatr. 1993. PMID: 8388447 Review.

5

Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.

Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ, Whiteman DA, et al. Weksberg R, et al. Hum Mol Genet. 1993 May;2(5):549-56. doi: 10.1093/hmg/2.5.549. Hum Mol Genet. 1993. PMID: 8518793

6

Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy.

Michaud JL, Héon E, Guilbert F, Weill J, Puech B, Benson L, Smallhorn JF, Shuman CT, Buncic JR, Levin AV, Weksberg R, Brevière GM. Michaud JL, et al. Among authors: weksberg r. J Pediatr. 1996 Feb;128(2):225-9. doi: 10.1016/s0022-3476(96)70394-3. J Pediatr. 1996. PMID: 8636816

7

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.

8

Molecular biology of Beckwith-Wiedemann syndrome.

Weksberg R, Squire JA. Weksberg R, et al. Med Pediatr Oncol. 1996 Nov;27(5):462-9. doi: 10.1002/(SICI)1096-911X(199611)27:5<462::AID-MPO13>3.0.CO;2-C. Med Pediatr Oncol. 1996. PMID: 8827075 Review.

9

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

10

Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities.

Moore CA, Toriello HV, Abuelo DN, Bull MJ, Curry CJ, Hall BD, Higgins JV, Stevens CA, Twersky S, Weksberg R, Dobyns WB. Moore CA, et al. Among authors: weksberg r. Am J Med Genet. 1997 May 2;70(1):67-73. Am J Med Genet. 1997. PMID: 9129744

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