Purvis-Smith S - Search Results

1

Duplication of 5q11.2----q13.1 from a familial (5;20) balanced insertion.

Yip MY, Kemp J, Hanson N, Wilson M, Purvis-Smith S, Lam-Po-Tang PR. Yip MY, et al. Among authors: purvis smith s. Am J Med Genet. 1989 Jun;33(2):220-3. doi: 10.1002/ajmg.1320330215. Am J Med Genet. 1989. PMID: 2764031

2

Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.

Yip MY, Selikowitz M, Don N, Kovacic A, Purvis-Smith S, Lam-Po-Tang PR. Yip MY, et al. Among authors: purvis smith s. J Med Genet. 1987 Nov;24(11):709-12. doi: 10.1136/jmg.24.11.709. J Med Genet. 1987. PMID: 3430549 Free PMC article.

3

Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.

Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR. Daniel A, et al. Am J Med Genet. 1982 Jan;11(1):61-75. doi: 10.1002/ajmg.1320110109. Am J Med Genet. 1982. PMID: 7065004

4

Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

Purvis-Smith SG, Saville T, Manass S, Yip MY, Lam-Po-Tang PR, Duffy B, Johnston H, Leigh D, McDonald B. Purvis-Smith SG, et al. Am J Hum Genet. 1992 Jun;50(6):1348-50. Am J Hum Genet. 1992. PMID: 1598916 Free PMC article. No abstract available.

5

Prenatal diagnosis of the fragile X--the Australasian experience.

Purvis-Smith SG, Laing S, Sutherland GR, Baker E. Purvis-Smith SG, et al. Am J Med Genet. 1988 May-Jun;30(1-2):337-45. doi: 10.1002/ajmg.1320300134. Am J Med Genet. 1988. PMID: 3177457

6

Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus sampling.

Callen DF, Korban G, Dawson G, Gugasyan L, Krumins EJ, Eichenbaum S, Petrass J, Purvis-Smith S, Smith A, Den Dulk G, et al. Callen DF, et al. Among authors: purvis smith s. Prenat Diagn. 1988 Jul;8(6):453-60. doi: 10.1002/pd.1970080610. Prenat Diagn. 1988. PMID: 3211847

7

Molecular distinction between true centric fission and pericentric duplication-fission.

Perry J, Nouri S, La P, Daniel A, Wu Z, Purvis-Smith S, Northrop E, Choo KH, Slater HR. Perry J, et al. Among authors: purvis smith s. Hum Genet. 2005 Mar;116(4):300-10. doi: 10.1007/s00439-004-1209-4. Epub 2005 Jan 27. Hum Genet. 2005. PMID: 15712016

8

Chromosomal localisation of a gene(s) for Turner stigmata on Yp.

Ogata T, Tyler-Smith C, Purvis-Smith S, Turner G. Ogata T, et al. Among authors: purvis smith s. J Med Genet. 1993 Nov;30(11):918-22. doi: 10.1136/jmg.30.11.918. J Med Genet. 1993. PMID: 8301645 Free PMC article. Review.

9

Chorionic villus sampling: cytogenetic experience in preliminary investigations and in 50 diagnostic cases.

Stewart LA, Purvis-Smith SG, Wass DM, Bennett MJ. Stewart LA, et al. Aust N Z J Obstet Gynaecol. 1986 Feb;26(1):71-5. doi: 10.1111/j.1479-828x.1986.tb01532.x. Aust N Z J Obstet Gynaecol. 1986. PMID: 3460576

10

Preventive screening for the fragile X syndrome.

Turner G, Robinson H, Laing S, Purvis-Smith S. Turner G, et al. Among authors: purvis smith s. N Engl J Med. 1986 Sep 4;315(10):607-9. doi: 10.1056/NEJM198609043151002. N Engl J Med. 1986. PMID: 3736599

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