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D Van Opstal

Showing results (11-20 of 42) with videos related to

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Fetal Diagnosis and Therapy|April 24, 2001
Prevalence of tetraploid metaphases in semidirect and cultured chorionic villiP Noomen, C van den Berg, J L de Ruyter, et al.
Prenatal Diagnosis|March 1, 1997
Full monosomy 21, prenatally diagnosed by fluorescent in situ hybridizationA M Joosten, S De Vos, D Van Opstal, et al.
Journal of Medical Genetics|August 1, 1995
Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletionJ O Van Hemel, C Schaap, D Van Opstal, et al.
Prenatal Diagnosis|November 14, 1997
Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studiesC Van den Berg, S K Ramlakhan, D Van Opstal, et al.
American Journal of Medical Genetics|December 11, 1996
Ring chromosome 18 in a fetus with only facial anomaliesF J Los, C van den Berg, P G Braat, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 4, 2014
Abnormal non-invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotypeM I Srebniak, K E M Diderich, P Noomen, et al.
Prenatal Diagnosis|March 29, 2014
SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))M I Srebniak, M J Bos, F A T de Vries, et al.
Prenatal Diagnosis|December 13, 2006
FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detectionE B Baart, I van den Berg, E Martini, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 31, 2013
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literatureM C de Wit, M I Srebniak, L C P Govaerts, et al.
Cancer Genetics and Cytogenetics|November 24, 1999
Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literatureG C Beverstock, P Mollevanger, M Baaij, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Fetal Diagnosis and Therapy|April 24, 2001
Prevalence of tetraploid metaphases in semidirect and cultured chorionic villiP Noomen, C van den Berg, J L de Ruyter, et al.
Prenatal Diagnosis|March 1, 1997
Full monosomy 21, prenatally diagnosed by fluorescent in situ hybridizationA M Joosten, S De Vos, D Van Opstal, et al.
Journal of Medical Genetics|August 1, 1995
Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletionJ O Van Hemel, C Schaap, D Van Opstal, et al.
Prenatal Diagnosis|November 14, 1997
Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studiesC Van den Berg, S K Ramlakhan, D Van Opstal, et al.
American Journal of Medical Genetics|December 11, 1996
Ring chromosome 18 in a fetus with only facial anomaliesF J Los, C van den Berg, P G Braat, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 4, 2014
Abnormal non-invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotypeM I Srebniak, K E M Diderich, P Noomen, et al.
Prenatal Diagnosis|March 29, 2014
SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))M I Srebniak, M J Bos, F A T de Vries, et al.
Prenatal Diagnosis|December 13, 2006
FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detectionE B Baart, I van den Berg, E Martini, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 31, 2013
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literatureM C de Wit, M I Srebniak, L C P Govaerts, et al.
Cancer Genetics and Cytogenetics|November 24, 1999
Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literatureG C Beverstock, P Mollevanger, M Baaij, et al.
Pageof 5