Stanier P - Search Results

1

Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome.

Monk D, Bentley L, Beechey C, Hitchins M, Peters J, Preece MA, Stanier P, Moore GE. Monk D, et al. Among authors: stanier p. J Med Genet. 2002 Aug;39(8):575-81. doi: 10.1136/jmg.39.8.575. J Med Genet. 2002. PMID: 12161597 Free PMC article. No abstract available.

2

Maternal uniparental disomy 7 in Silver-Russell syndrome.

Preece MA, Price SM, Davies V, Clough L, Stanier P, Trembath RC, Moore GE. Preece MA, et al. Among authors: stanier p. J Med Genet. 1997 Jan;34(1):6-9. doi: 10.1136/jmg.34.1.6. J Med Genet. 1997. PMID: 9032641 Free PMC article.

3

Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome.

Wakeling EL, Hitchins MP, Abu-Amero SN, Stanier P, Moore GE, Preece MA. Wakeling EL, et al. Among authors: stanier p. J Med Genet. 2000 Jan;37(1):65-7. doi: 10.1136/jmg.37.1.65. J Med Genet. 2000. PMID: 10691413 Free PMC article. No abstract available.

4

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands.

Preece MA, Abu-Amero SN, Ali Z, Abu-Amero KK, Wakeling EL, Stanier P, Moore GE. Preece MA, et al. Among authors: stanier p. J Med Genet. 1999 Jun;36(6):457-60. J Med Genet. 1999. PMID: 10874633 Free PMC article.

5

Silver-Russell syndrome and ring chromosome 7.

Wakeling EL, Hitchins M, Stanier P, Monk D, Moore GE, Preece MA. Wakeling EL, et al. Among authors: stanier p. J Med Genet. 2000 May;37(5):380. doi: 10.1136/jmg.37.5.380. J Med Genet. 2000. PMID: 10905891 Free PMC article. No abstract available.

6

No evidence for mosaicism in Silver-Russell syndrome.

Monk D, Hitchins M, Russo S, Preece M, Stanier P, Moore GE. Monk D, et al. Among authors: stanier p. J Med Genet. 2001 Apr;38(4):E11. doi: 10.1136/jmg.38.4.e11. J Med Genet. 2001. PMID: 11283207 Free PMC article. No abstract available.

7

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Hitchins MP, Stanier P, Preece MA, Moore GE. Hitchins MP, et al. Among authors: stanier p. J Med Genet. 2001 Dec;38(12):810-9. doi: 10.1136/jmg.38.12.810. J Med Genet. 2001. PMID: 11748303 Free PMC article. Review.

8

Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q.

Hitchins MP, Abu-Amero S, Apostolidou S, Monk D, Stanier P, Preece MA, Moore GE. Hitchins MP, et al. Among authors: stanier p. J Med Genet. 2002 Mar;39(3):E13. doi: 10.1136/jmg.39.3.e13. J Med Genet. 2002. PMID: 11897833 Free PMC article. No abstract available.

9

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.

Bentley L, Nakabayashi K, Monk D, Beechey C, Peters J, Birjandi Z, Khayat FE, Patel M, Preece MA, Stanier P, Scherer SW, Moore GE. Bentley L, et al. Among authors: stanier p. J Med Genet. 2003 Apr;40(4):249-56. doi: 10.1136/jmg.40.4.249. J Med Genet. 2003. PMID: 12676894 Free PMC article.

10

The genetic aetiology of Silver-Russell syndrome.

Abu-Amero S, Monk D, Frost J, Preece M, Stanier P, Moore GE. Abu-Amero S, et al. Among authors: stanier p. J Med Genet. 2008 Apr;45(4):193-9. doi: 10.1136/jmg.2007.053017. Epub 2007 Dec 21. J Med Genet. 2008. PMID: 18156438 Review.

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