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R Hochstenbach

Showing results (21-30 of 27) with videos related to

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Prenatal Diagnosis|April 9, 2008
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriageM T M Franssen, J C Korevaar, W M Tjoa, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens, D A Scott, M van Dooren, et al.
Prenatal Diagnosis|October 19, 2005
Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)R Hochstenbach, J Meijer, J van de Brug, et al.
Clinical Genetics|October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disordersH M Ozgen, E van Daalen, P F Bolton, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 3, 2007
[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping]M T M Franssen, J C Korevaar, N J Leschot, et al.
Journal of Intellectual Disability Research : JIDR|March 7, 2017
Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the NetherlandsG de Graaf, J J M Engelen, A C J Gijsbers, et al.
Case Reports in Genetics|July 3, 2015
Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18R Hochstenbach, G C M L Page-Christiaens, A C C van Oppen, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Prenatal Diagnosis|April 9, 2008
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriageM T M Franssen, J C Korevaar, W M Tjoa, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens, D A Scott, M van Dooren, et al.
Prenatal Diagnosis|October 19, 2005
Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)R Hochstenbach, J Meijer, J van de Brug, et al.
Clinical Genetics|October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disordersH M Ozgen, E van Daalen, P F Bolton, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 3, 2007
[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping]M T M Franssen, J C Korevaar, N J Leschot, et al.
Journal of Intellectual Disability Research : JIDR|March 7, 2017
Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the NetherlandsG de Graaf, J J M Engelen, A C J Gijsbers, et al.
Case Reports in Genetics|July 3, 2015
Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18R Hochstenbach, G C M L Page-Christiaens, A C C van Oppen, et al.
Pageof 3