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A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary events.
Published in:
1980
By:
- Hustinx, T. W. J.;
- Burghouts, J. T. M.;
- Scheres, J. M. J. C.;
- Smits, A. P. T.;
- Hustinx, T W;
- Burghouts, J T;
- Scheres, J M;
- Smits, A P
Publication type:
journal article
Women's Attitudes towards the Option to Choose between Karyotyping and Rapid Targeted Testing during Pregnancy.
Published in:
Obstetrics & Gynecology International, 2013, p. 1, doi. 10.1155/2013/636459
By:
- Kooper, Angelique J. A.;
- Smeets, Dominique F. C. M.;
- Feenstra, Ilse;
- Wijnberger, Lia D. E.;
- Rijnders, Robbert J. P.;
- Quartero, Rik W. P.;
- Boekkooi, Peter F.;
- van Vugt, John M. G.;
- Smits, Arie P. T.
Publication type:
Article
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34.
Published in:
European Journal of Human Genetics, 2003, v. 11, n. 5, p. 409, doi. 10.1038/sj.ejhg.5200982
By:
- Galjaard, Robert-Jan H;
- Smits, Arie P T;
- Tuerlings, Joep H A M;
- Bais, Aagje G;
- Avella, Aida M Bertoli;
- Breedveld, Guido;
- Graaff, Esther de;
- Oostra, Ben A;
- Heutink, Peter
Publication type:
Article
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23–q24.
Published in:
European Journal of Human Genetics, 1998, v. 6, n. 4, p. 376, doi. 10.1038/sj.ejhg.5200229
By:
- van der Vleuten, A J W;
- van Ravenswaaij-Arts, C M A;
- Frijns, C J M;
- Smits, A P T;
- Hageman, G;
- Padberg, G W;
- Kremer, H
Publication type:
Article
Why do parents prefer to know the fetal sex as part of invasive prenatal testing?
Published in:
2012
By:
- Kooper, Angelique J. A.;
- Pieters, Jacqueline J. P. M.;
- Eggink, Alex J.;
- Feuth, Ton B.;
- Feenstra, Ilse;
- Wijnberger, Lia D. E.;
- Rijnders, Robbert J. P.;
- Quartero, Rik W. P.;
- Boekkooi, Peter F.;
- van Vugt, John M. G.;
- Smits, Arie P. T.
Publication type:
journal article
Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior, and fertility.
Published in:
2011
By:
- Pieters, J J P M;
- Kooper, A J A;
- van Kessel, A Geurts;
- Braat, D D M;
- Smits, A P T
Publication type:
journal article
Monosomy 7 in Two Patients with a Myeloproliferative Disorder.
Published in:
British Journal of Haematology, 1977, v. 37, n. 1, p. 101, doi. 10.1111/j.1365-2141.1977.tb08815.x
By:
- Boetius, G.;
- Hustinx, T. W. J.;
- Smits, A. P. T.;
- Scheres, M.J. C.;
- Rutten, F.J.;
- Haanen, C.
Publication type:
Article
Experts' opinions on the benefit of an incidental prenatal diagnosis of sex chromosomal aneuploidy: a qualitative interview survey.
Published in:
Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1151, doi. 10.1002/pd.3975
By:
- Pieters, J. J. P. M.;
- Verhaak, C. M.;
- Braat, D. D. M.;
- Leeuwen, E.;
- Smits, A. P. T.
Publication type:
Article
Parents' perspectives on the unforeseen finding of a fetal sex chromosomal aneuploidy.
Published in:
Prenatal Diagnosis, 2011, v. 31, n. 3, p. 286, doi. 10.1002/pd.2707
By:
- Pieters, J. J. P. M.;
- Kooper, A. J. A.;
- Eggink, A. J.;
- Verhaak, C. M.;
- Otten, B. J.;
- Braat, D. D. M.;
- Smits, A. P. T.;
- van Leeuwen, E.
Publication type:
Article
Multiplex Ligation-dependent Probe Amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells.
Published in:
Prenatal Diagnosis, 2008, v. 28, n. 11, p. 1004, doi. 10.1002/pd.2111
By:
- Kooper, Angelique J. A.;
- Faas, Brigitte H. W.;
- Kater-Baats, Ellen;
- Feuth, Ton;
- Janssen, Jasper C. J. A.;
- van der Burgt, Ineke;
- Lotgering, Fred K.;
- Geurts van Kessel, Ad;
- Smits, Arie P. T.
Publication type:
Article
Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defects.
Published in:
2007
By:
- Kooper, Angelique J. A.;
- de Bruijn, Dagmar;
- van Ravenwaaij-Arts, Conny M. A.;
- Faas, Brigitte H. W.;
- Creemers, Johan W. T.;
- Thomas, Chris M. G.;
- Smits, Arie P. T.
Publication type:
journal article

Found: 11