Binder G - Search Results

1

IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia.

Zeschnigk M, Albrecht B, Buiting K, Kanber D, Eggermann T, Binder G, Gromoll J, Prott EC, Seland S, Horsthemke B. Zeschnigk M, et al. Among authors: binder g. Eur J Hum Genet. 2008 Mar;16(3):328-34. doi: 10.1038/sj.ejhg.5201974. Epub 2008 Jan 9. Eur J Hum Genet. 2008. PMID: 18159214

2

MBD3 mutations are not responsible for ICR1 hypomethylation in Silver-Russell syndrome.

Bachmann N, Spengler S, Binder G, Eggermann T. Bachmann N, et al. Among authors: binder g. Eur J Med Genet. 2010 Jan-Feb;53(1):23-4. doi: 10.1016/j.ejmg.2009.12.002. Epub 2009 Dec 16. Eur J Med Genet. 2010. PMID: 20004753

3

Screening for insulin-like growth factor-I receptor mutations in patients with Silver-Russell syndrome.

Binder G, Mavridou K, Wollmann HA, Eggermann T, Ranke MB. Binder G, et al. J Pediatr Endocrinol Metab. 2002 Sep-Oct;15(8):1167-71. doi: 10.1515/jpem.2002.15.8.1167. J Pediatr Endocrinol Metab. 2002. PMID: 12387515

4

The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration.

Binder G, Seidel AK, Martin DD, Schweizer R, Schwarze CP, Wollmann HA, Eggermann T, Ranke MB. Binder G, et al. J Clin Endocrinol Metab. 2008 Apr;93(4):1402-7. doi: 10.1210/jc.2007-1897. Epub 2008 Jan 29. J Clin Endocrinol Metab. 2008. PMID: 18230663

5

No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation.

Schönherr N, Meyer E, Binder G, Wollmann HA, Eggermann T. Schönherr N, et al. Among authors: binder g. J Pediatr Endocrinol Metab. 2007 Dec;20(12):1329-31. doi: 10.1515/jpem.2007.20.12.1329. J Pediatr Endocrinol Metab. 2007. PMID: 18341093

6

No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patients.

Schöherr N, Jäger S, Ranke MB, Wollmann HA, Binder G, Eggermann T. Schöherr N, et al. Among authors: binder g. Eur J Med Genet. 2008 Jul-Aug;51(4):322-4. doi: 10.1016/j.ejmg.2008.05.001. Epub 2008 May 23. Eur J Med Genet. 2008. PMID: 18585117

7

Are H19 variants associated with Silver-Russell syndrome?

Schönherr N, Binder G, Korsch E, Kämmerer E, Wollmann HA, Eggermann T. Schönherr N, et al. Among authors: binder g. J Pediatr Endocrinol Metab. 2008 Oct;21(10):985-93. doi: 10.1515/jpem.2008.21.10.985. J Pediatr Endocrinol Metab. 2008. PMID: 19209620

8

Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations.

Spengler S, Gogiel M, Schönherr N, Binder G, Eggermann T. Spengler S, et al. Among authors: binder g. Eur J Med Genet. 2009 Nov-Dec;52(6):415-6. doi: 10.1016/j.ejmg.2009.07.005. Epub 2009 Jul 24. Eur J Med Genet. 2009. PMID: 19632365

9

Silver-Russell syndrome: genetic basis and molecular genetic testing.

Eggermann T, Begemann M, Binder G, Spengler S. Eggermann T, et al. Among authors: binder g. Orphanet J Rare Dis. 2010 Jun 23;5:19. doi: 10.1186/1750-1172-5-19. Orphanet J Rare Dis. 2010. PMID: 20573229 Free PMC article. Review.

10

Silver-Russell syndrome.

Binder G, Begemann M, Eggermann T, Kannenberg K. Binder G, et al. Best Pract Res Clin Endocrinol Metab. 2011 Feb;25(1):153-60. doi: 10.1016/j.beem.2010.06.005. Best Pract Res Clin Endocrinol Metab. 2011. PMID: 21396582

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