Monk D - Search Results

1

Diagnosis and management of Silver-Russell syndrome: first international consensus statement.

Wakeling EL, Brioude F, Lokulo-Sodipe O, O'Connell SM, Salem J, Bliek J, Canton AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Grønskov K, Hokken-Koelega AC, Jorge AA, Kagami M, Linglart A, Maghnie M, Mohnike K, Monk D, Moore GE, Murray PG, Ogata T, Petit IO, Russo S, Said E, Toumba M, Tümer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I. Wakeling EL, et al. Among authors: monk d. Nat Rev Endocrinol. 2017 Feb;13(2):105-124. doi: 10.1038/nrendo.2016.138. Epub 2016 Sep 2. Nat Rev Endocrinol. 2017. PMID: 27585961

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

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.

6

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

7

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

8

DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.

Hitchins MP, Bentley L, Monk D, Beechey C, Peters J, Kelsey G, Ishino F, Preece MA, Stanier P, Moore GE. Hitchins MP, et al. Among authors: monk d. Mamm Genome. 2002 Dec;13(12):686-91. doi: 10.1007/s00335-002-3028-z. Mamm Genome. 2002. PMID: 12514746

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: 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.

10

Intrauterine growth restriction--genetic causes and consequences.

Monk D, Moore GE. Monk D, et al. Semin Fetal Neonatal Med. 2004 Oct;9(5):371-8. doi: 10.1016/j.siny.2004.03.002. Semin Fetal Neonatal Med. 2004. PMID: 15691772 Review.

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