Hitchins M - Search Results

1

Positive association in the absence of linkage suggests a minor role for the glucokinase gene in the pathogenesis of type 2 (non-insulin-dependent) diabetes mellitus amongst south Indians.

McCarthy MI, Hitchins M, Hitman GA, Cassell P, Hawrami K, Morton N, Mohan V, Ramachandran A, Snehalatha C, Viswanathan M. McCarthy MI, et al. Among authors: hitchins m. Diabetologia. 1993 Jul;36(7):633-41. doi: 10.1007/BF00404073. Diabetologia. 1993. PMID: 8359581

2

Glucokinase gene polymorphisms: a genetic marker for glucose intolerance in a cohort of elderly Finnish men.

McCarthy MI, Hitman GA, Hitchins M, Riikonen A, Stengård J, Nissinen A, Tuomilehto-Wolf E, Tuomilehto J. McCarthy MI, et al. Among authors: hitchins m. Diabet Med. 1994 Mar;11(2):198-204. doi: 10.1111/j.1464-5491.1994.tb02020.x. Diabet Med. 1994. PMID: 8200207

3

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: hitchins m. 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.

4

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. Eur J Hum Genet. 2001 Feb;9(2):82-90. doi: 10.1038/sj.ejhg.5200583. Eur J Hum Genet. 2001. PMID: 11313740

5

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. Among authors: hitchins m. 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

6

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. Among authors: hitchins m. Am J Hum Genet. 2000 Jan;66(1):36-46. doi: 10.1086/302717. Am J Hum Genet. 2000. PMID: 10631135 Free PMC article.

7

Genomic imprinting in fetal growth and development.

Hitchins MP, Moore GE. Hitchins MP, et al. Expert Rev Mol Med. 2002 May 9;4(11):1-19. doi: 10.1017/S146239940200457X. Expert Rev Mol Med. 2002. PMID: 14987379 Review.

8

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: hitchins mp. 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.

9

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. 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.

10

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: hitchins m. 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.

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