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Prenatal Diagnosis
|
April 9, 2008
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage
M 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-qter
M 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 disorders
H 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 Netherlands
G 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 18
R Hochstenbach, G C M L Page-Christiaens, A C C van Oppen, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 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 miscarriage
M 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-qter
M 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 disorders
H 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 Netherlands
G 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 18
R Hochstenbach, G C M L Page-Christiaens, A C C van Oppen, et al.
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of 3