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Nederlands Tijdschrift Voor Geneeskunde|October 9, 2002
[Perinatal asphyxia as incorrect explanation for mental retardation]J H A M Tuerlings, A P T Smits, P P van den BergPrenatal Diagnosis|October 2, 2012
Experts' opinions on the benefit of an incidental prenatal diagnosis of sex chromosomal aneuploidy: a qualitative interview surveyJ J P M Pieters, C M Verhaak, D D M Braat, et al.American Journal of Medical Genetics. Part A|January 28, 2003
Female carriers of fragile X premutations have no increased risk for additional diseases other than premature ovarian failureR D L Hundscheid, A P T Smits, C M G Thomas, et al.ISRN Obstetrics and Gynecology|December 23, 2011
Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior, and fertilityJ J P M Pieters, A J A Kooper, A Geurts van Kessel, et al.Genetic Counseling (Geneva, Switzerland)|April 28, 2010
A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case reportF E P Mundhofir, A J A Kooper, T I Winarni, et al.Journal of Medical Genetics|June 26, 2010
Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysisB H W Faas, I van der Burgt, A J A Kooper, et al.Prenatal Diagnosis|February 5, 2011
Parents' perspectives on the unforeseen finding of a fetal sex chromosomal aneuploidyJ J P M Pieters, A J A Kooper, A J Eggink, et al.Human Reproduction (Oxford, England)|May 18, 2011
Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriersM A Spath, T B Feuth, E G Allen, et al.Nederlands Tijdschrift Voor Geneeskunde|September 16, 2008
[Alpha-foetoprotein assessment in amniotic fluid for the detection of neural tube defects: limited added value beyond week 20 ultrasound; retrospective study]A J A Kooper, A P T Smits, A B Feuth, et al.Pageof 1