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Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.
Published in:
Clinical Genetics, 2006, v. 69, n. 1, p. 86, doi. 10.1111/j.1399-0004.2006.00552.x
By:
- Verdyck, P.;
- Blaumeiser, B.;
- Holder-Espinasse, M.;
- Van Hul, W.;
- W. Wuyts
Publication type:
Article
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 ( FCRL3) gene in alopecia areata.
Published in:
International Journal of Immunogenetics, 2006, v. 33, n. 6, p. 393, doi. 10.1111/j.1744-313X.2006.00633.x
By:
- Schäfer, N.;
- Blaumeiser, B.;
- Becker, T.;
- Freudenberg-Hua, Y.;
- Hanneken, S.;
- Eigelshoven, S.;
- Schmael, C.;
- Lambert, J.;
- De Weert, J.;
- Kruse, R.;
- Nöthen, M. M.;
- Betz, R. C.
Publication type:
Article
VP06.11: Difference in procedure‐related risk of miscarriage between early and mid‐trimester amniocentesis: a retrospective cohort study.
Published in:
Ultrasound in Obstetrics & Gynecology, 2020, v. 56, p. 78, doi. 10.1002/uog.22423
By:
- Steinfort, K.;
- Van Houtven, E.;
- Loquet, P.;
- Blaumeiser, B.;
- Jacquemyn, Y.
Publication type:
Article
Abstracts of the 26th World Congress on Ultrasound in Obstetrics and Gynecology, Rome, Italy, 24-28 September 2016.
Published in:
2016
By:
- Muys, J.;
- Blaumeiser, B.;
- Janssens, K.;
- Bandelier, C.;
- Gatot, J.;
- Van Den Bogaert, A.;
- Vermeesch, J.;
- Rombout, S.;
- Menten, B.;
- Pichon, B.;
- Keymolen, K.;
- Van Den Bogaert, K.;
- Janssens, S.;
- Caberg, J.;
- Désir, J.;
- Sznajer, Y.;
- Destree, A.;
- Jacquemyn, Y.;
- Désir, J
Publication type:
journal article
Additional causal SNRPE mutations in hereditary hypotrichosis simplex.
Published in:
British Journal of Dermatology, 2021, v. 185, n. 2, p. 439, doi. 10.1111/bjd.20089
By:
- Pan, C.;
- Humbatova, A.;
- Zheng, L.;
- Cesarato, N.;
- Grimm, C.;
- Chen, F.;
- Blaumeiser, B.;
- Catalán‐Lambán, A.;
- Patiño‐García, A.;
- Fischer, U.;
- Cheng, R.;
- Li, Y.;
- Yu, X.;
- Yao, Z.;
- Li, M.;
- Betz, R.C.
Publication type:
Article
Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testing.
Published in:
2012
By:
- Leeneer, K.;
- Bockstal, M.;
- Brouwer, S.;
- Swietek, N.;
- Schietecatte, P.;
- Sabbaghian, N.;
- den Ende, J.;
- Willocx, S.;
- Storm, K.;
- Blaumeiser, B.;
- Asperen, C.;
- Wijnen, J.;
- Leunen, K.;
- Legius, E.;
- Michils, G.;
- Matthijs, G.;
- Blok, M.;
- Gomez-Garcia, E.;
- Paepe, A.;
- Tischkowitz, M.
Publication type:
Report
Disclosure Pattern and Follow-Up After the Molecular Diagnosis of BRCA/CHEK2 Mutations.
Published in:
Journal of Genetic Counseling, 2014, v. 23, n. 2, p. 254, doi. 10.1007/s10897-013-9656-5
By:
- Kegelaers, D.;
- Merckx, W.;
- Odeurs, P.;
- Ende, J.;
- Blaumeiser, B.
Publication type:
Article
Outcome of preimplantation genetic diagnosis for genetic disease.
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, p. S-49
By:
- S., Gordts;
- V., Frederickx;
- G., Van Kerkhoven;
- P., Roziers;
- R., Campo;
- P., Puttemans;
- M., Valkenburg;
- C., Magli;
- L., Gianaroli;
- B., Blaumeiser;
- J., Wauters
Publication type:
Article
Is preimplantation genetic screening useful in repeated IVF failure group?
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, p. S-23, doi. 10.1016/S1472-6483(10)61353-3
By:
- S., Gordts;
- V., Frederickx;
- G., Van Kerkhoven;
- P., Roziers;
- R., Campo;
- P., Puttemans;
- M., Valkenburg;
- C., Magli;
- L., Gianaroli;
- B., Blaumeiser;
- J., Wauters
Publication type:
Article
Invasive papillary carcinoma of the male breast.
Published in:
2002
By:
- Blaumeiser, B.;
- Tjalma, W.;
- Verslegers, I.;
- Schepper, De A.;
- Buytaert, P.;
- Tjalma, W A A;
- De Schepper, A M
Publication type:
journal article
Investigation of selected cytokine genes suggests that IL2RA and the TNF/ LTA locus are risk factors for severe alopecia areata.
Published in:
British Journal of Dermatology, 2012, v. 167, n. 6, p. 1360, doi. 10.1111/bjd.12004
By:
- Redler, S.;
- Albert, F.;
- Brockschmidt, F.F.;
- Herold, C.;
- Hanneken, S.;
- Eigelshoven, S.;
- Giehl, K.A.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Blaumeiser, B.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Betz, R.C.
Publication type:
Article
The TRAF1/C5 locus confers risk for familial and severe alopecia areata.
Published in:
British Journal of Dermatology, 2010, v. 162, n. 4, p. 866, doi. 10.1111/j.1365-2133.2009.09598.x
By:
- Redler, S.;
- Brockschmidt, F.F.;
- Forstbauer, L.;
- Giehl, K.A.;
- Herold, C.;
- Eigelshoven, S.;
- Hanneken, S.;
- De Weert, J.;
- Lutz, G.;
- Wolff, H.;
- Kruse, R.;
- Blaumeiser, B.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Betz, R.C.
Publication type:
Article
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.
Published in:
British Journal of Dermatology, 2008, v. 158, n. 2, p. 389, doi. 10.1111/j.1365-2133.2007.08312.x
By:
- Betz, Regina C.;
- König, K.;
- Flaquer, A.;
- Redler, S.;
- Eigelshoven, S.;
- Kortüm, A.-K.;
- Hanneken, S.;
- Hillmer, A.;
- Tüting, T.;
- Lambert, J.;
- De Weert, J.;
- Kruse, R.;
- Lutz, G.;
- Blaumeiser, B.;
- Nöthen, M. M.
Publication type:
Article

Found: 13