Ranke MB - Search Results

1

Segmental uniparental disomy of 7q31-qter is rare in Silver-Russell syndrome.

Eggermann T, Mergenthaler S, Eggermann K, Ranke MB, Wollmann HA. Eggermann T, et al. Among authors: ranke mb. Clin Genet. 2001 Nov;60(5):395-6. doi: 10.1034/j.1399-0004.2001.600514.x. Clin Genet. 2001. PMID: 11903344 No abstract available.

2

IRS1 and GRB2 as members of the IGF signal transduction pathway are not associated with intrauterine growth retardation and Silver-Russell syndrome.

Eggermann T, Kloos P, Mergenthaler S, Eggermann K, Dobos M, Ranke M, Wollmann H. Eggermann T, et al. Clin Genet. 2001 May;59(5):371-3. doi: 10.1034/j.1399-0004.2001.590515.x. Clin Genet. 2001. PMID: 11359473 No abstract available.

3

Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome.

Eggermann T, Schönherr N, Eggermann K, Buiting K, Ranke MB, Wollmann HA, Binder G. Eggermann T, et al. Among authors: ranke mb. Clin Genet. 2008 Jan;73(1):79-84. doi: 10.1111/j.1399-0004.2007.00930.x. Epub 2007 Dec 7. Clin Genet. 2008. PMID: 18070127

4

Segmental maternal UPD(7q) in Silver-Russell syndrome.

Eggermann T, Schönherr N, Jäger S, Spaich C, Ranke MB, Wollmann HA, Binder G. Eggermann T, et al. Among authors: ranke mb. Clin Genet. 2008 Nov;74(5):486-9. doi: 10.1111/j.1399-0004.2008.01057.x. Epub 2008 Aug 12. Clin Genet. 2008. PMID: 18700897 No abstract available.

5

Characterization of genomic variants in CSH1 and GH2, two candidate genes for Silver-Russell syndrome in 17q24-q25.

Prager S, Wollmann HA, Mergenthaler S, Mavany M, Eggermann K, Ranke MB, Eggermann T. Prager S, et al. Among authors: ranke mb. Genet Test. 2003 Fall;7(3):259-63. doi: 10.1089/109065703322537304. Genet Test. 2003. PMID: 14642004

6

Diagnostic proceeding in Silver-Russell syndrome.

Eggermann T, Meyer E, Ranke MB, Holder M, Spranger S, Zerres K, Wollmann HA. Eggermann T, et al. Among authors: ranke mb. Mol Diagn. 2005;9(4):205-9. doi: 10.1007/BF03260093. Mol Diagn. 2005. PMID: 16392900

7

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. Among authors: ranke mb. 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

8

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: ranke mb. 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

9

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

Eggermann T, Wollmann HA, Kuner R, Eggermann K, Enders H, Kaiser P, Ranke MB. Eggermann T, et al. Among authors: ranke mb. Hum Genet. 1997 Sep;100(3-4):415-9. doi: 10.1007/s004390050526. Hum Genet. 1997. PMID: 9272165

10

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.

Eggermann T, Eggermann K, Mergenthaler S, Kuner R, Kaiser P, Ranke MB, Wollmann HA. Eggermann T, et al. Among authors: ranke mb. J Med Genet. 1998 Sep;35(9):784-6. doi: 10.1136/jmg.35.9.784. J Med Genet. 1998. PMID: 9733042 Free PMC article.

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