Moog U - Search Results

1

Impact of BRCA1/2 testing and disclosure of a positive test result on women affected and unaffected with breast or ovarian cancer.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: moog u. Am J Med Genet A. 2004 Feb 1;124A(4):346-55. doi: 10.1002/ajmg.a.20374. Am J Med Genet A. 2004. PMID: 14735581 Free article.

2

Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: moog u. Br J Cancer. 2004 Jan 26;90(2):333-42. doi: 10.1038/sj.bjc.6601525. Br J Cancer. 2004. PMID: 14735173 Free PMC article. Clinical Trial.

3

Randomized trial of a shared decision-making intervention consisting of trade-offs and individualized treatment information for BRCA1/2 mutation carriers.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: moog u. J Clin Oncol. 2004 Aug 15;22(16):3293-301. doi: 10.1200/JCO.2004.05.066. J Clin Oncol. 2004. PMID: 15310772 Free article. Clinical Trial.

4

The decision evaluation scales.

Stalmeier PF, Roosmalen MS, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Moog U, Hoogerbrugge N, van Daal WA. Stalmeier PF, et al. Among authors: moog u. Patient Educ Couns. 2005 Jun;57(3):286-93. doi: 10.1016/j.pec.2004.07.010. Patient Educ Couns. 2005. PMID: 15893210 Free article.

5

The outcome of diagnostic studies on the etiology of mental retardation: considerations on the classification of the causes.

Moog U. Moog U. Am J Med Genet A. 2005 Aug 30;137(2):228-31. doi: 10.1002/ajmg.a.30841. Am J Med Genet A. 2005. PMID: 16086396 Review.

6

Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?

Moog U, Maroteaux P, Schrander-Stumpel CT, van Ooij A, Schrander JJ, Fryns JP. Moog U, et al. J Med Genet. 1999 Nov;36(11):856-8. J Med Genet. 1999. PMID: 10544232 Free PMC article.

7

Acampomelic campomelic syndrome.

Moog U, Jansen NJ, Scherer G, Schrander-Stumpel CT. Moog U, et al. Am J Med Genet. 2001 Dec 1;104(3):239-45. Am J Med Genet. 2001. PMID: 11754051

8

Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?

Moog U, Bleeker-Wagemakers EM, Crobach P, Vles JS, Schrander-Stumpel CT. Moog U, et al. Am J Med Genet. 1998 Jul 7;78(3):263-6. Am J Med Genet. 1998. PMID: 9677063

9

Epidermolysis bullosa simplex with mottled pigmentation: clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patients.

Moog U, de Die-Smulders CE, Scheffer H, van der Vlies P, Henquet CJ, Jonkman MF. Moog U, et al. Am J Med Genet. 1999 Oct 8;86(4):376-9. doi: 10.1002/(sici)1096-8628(19991008)86:4<376::aid-ajmg12>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10494094

10

ICF syndrome: a new case and review of the literature.

Smeets DF, Moog U, Weemaes CM, Vaes-Peeters G, Merkx GF, Niehof JP, Hamers G. Smeets DF, et al. Among authors: moog u. Hum Genet. 1994 Sep;94(3):240-6. doi: 10.1007/BF00208277. Hum Genet. 1994. PMID: 8076938 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

142 results

Search Page

Filters