Monk D - Search Results

1

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: monk d. 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.

2

The search for the gene for Silver-Russell syndrome.

Moore GE, Abu-Amero S, Wakeling E, Hitchins M, Monk D, Stanier P, Preece M. Moore GE, et al. Among authors: monk d. Acta Paediatr Suppl. 1999 Dec;88(433):42-8. doi: 10.1111/j.1651-2227.1999.tb14402.x. Acta Paediatr Suppl. 1999. PMID: 10626544 Review.

3

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.

Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, Preece MA, Moore GE. Monk D, et al. Am J Hum Genet. 2000 Jan;66(1):36-46. doi: 10.1086/302717. Am J Hum Genet. 2000. PMID: 10631135 Free PMC article.

4

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: monk d. 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.

5

Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?

Mergenthaler S, Hitchins MP, Blagitko-Dorfs N, Monk D, Wollmann HA, Ranke MB, Ropers HH, Apostolidou S, Stanier P, Preece MA, Eggermann T, Kalscheuer VM, Moore GE. Mergenthaler S, et al. Among authors: monk d. Am J Hum Genet. 2001 Feb;68(2):543-5. doi: 10.1086/318192. Am J Hum Genet. 2001. PMID: 11170901 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. 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

Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.

Hitchins MP, Monk D, Bell GM, Ali Z, Preece MA, Stanier P, Moore GE. Hitchins MP, et al. Among authors: monk d. Eur J Hum Genet. 2001 Feb;9(2):82-90. doi: 10.1038/sj.ejhg.5200583. Eur J Hum Genet. 2001. PMID: 11313740

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: monk d. 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

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. 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.

10

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE. Monk D, et al. Hum Genet. 2002 Oct;111(4-5):376-87. doi: 10.1007/s00439-002-0777-4. Epub 2002 Aug 16. Hum Genet. 2002. PMID: 12384779

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