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Human Reproduction (Oxford, England)
|
August 1, 1995
The use of epididymal and testicular spermatozoa for intracytoplasmic sperm injection: the genetic implications for male infertility
S J Silber, Z Nagy, J Liu, et al.
European Journal of Pediatrics
|
September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene
W Lissens, P Vreken, P G Barth, et al.
Acta Obstetricia Et Gynecologica Scandinavica
|
January 1, 1986
Pathological pregnancies. Results of amniotic fluid studies and fetal outcome
N Van Regemorter, E Vamos, V Defleur, et al.
Human Reproduction (Oxford, England)
|
January 6, 2007
Single embryo transfer in preimplantation genetic diagnosis cycles for women <36 years does not reduce delivery rate
P Donoso, W Verpoest, E G Papanikolaou, et al.
Journal of Assisted Reproduction and Genetics
|
July 1, 1993
Current progress in preimplantation genetic diagnosis
Y Verlinsky, A Handyside, J L Simpson, et al.
Human Reproduction (Oxford, England)
|
December 9, 2010
Closed blastocyst vitrification of biopsied embryos: evaluation of 100 consecutive warming cycles
L Van Landuyt, W Verpoest, G Verheyen, et al.
Human Reproduction Open
|
March 22, 2019
Body composition and blood pressure in 6-year-old singletons born after pre-implantation genetic testing for monogenic and structural chromosomal aberrations: a matched cohort study
F Belva, M Roelants, S Kluijfhout, et al.
Molecular Human Reproduction
|
September 11, 1998
Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)
K Sermon, A De Vos, H Van de Velde, et al.
Human Reproduction (Oxford, England)
|
March 5, 2004
Novel universal approach for preimplantation genetic diagnosis of beta-thalassaemia in combination with HLA matching of embryos
H Van de Velde, I Georgiou, M De Rycke, et al.
Pediatric Research
|
December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathy
L De Meirleir, W Lissens, C Benelli, et al.
Page
of 22
Search research articles
Search
Showing results (171-180 of 211) with videos related to
Sort By:
Page
of 22
Human Reproduction (Oxford, England)
|
August 1, 1995
The use of epididymal and testicular spermatozoa for intracytoplasmic sperm injection: the genetic implications for male infertility
S J Silber, Z Nagy, J Liu, et al.
European Journal of Pediatrics
|
September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene
W Lissens, P Vreken, P G Barth, et al.
Acta Obstetricia Et Gynecologica Scandinavica
|
January 1, 1986
Pathological pregnancies. Results of amniotic fluid studies and fetal outcome
N Van Regemorter, E Vamos, V Defleur, et al.
Human Reproduction (Oxford, England)
|
January 6, 2007
Single embryo transfer in preimplantation genetic diagnosis cycles for women <36 years does not reduce delivery rate
P Donoso, W Verpoest, E G Papanikolaou, et al.
Journal of Assisted Reproduction and Genetics
|
July 1, 1993
Current progress in preimplantation genetic diagnosis
Y Verlinsky, A Handyside, J L Simpson, et al.
Human Reproduction (Oxford, England)
|
December 9, 2010
Closed blastocyst vitrification of biopsied embryos: evaluation of 100 consecutive warming cycles
L Van Landuyt, W Verpoest, G Verheyen, et al.
Human Reproduction Open
|
March 22, 2019
Body composition and blood pressure in 6-year-old singletons born after pre-implantation genetic testing for monogenic and structural chromosomal aberrations: a matched cohort study
F Belva, M Roelants, S Kluijfhout, et al.
Molecular Human Reproduction
|
September 11, 1998
Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)
K Sermon, A De Vos, H Van de Velde, et al.
Human Reproduction (Oxford, England)
|
March 5, 2004
Novel universal approach for preimplantation genetic diagnosis of beta-thalassaemia in combination with HLA matching of embryos
H Van de Velde, I Georgiou, M De Rycke, et al.
Pediatric Research
|
December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathy
L De Meirleir, W Lissens, C Benelli, et al.
Page
of 22