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Human Reproduction Open
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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.
Human Reproduction (Oxford, England)
|
July 17, 2008
Neonatal outcome of 937 children born after transfer of cryopreserved embryos obtained by ICSI and IVF and comparison with outcome data of fresh ICSI and IVF cycles
F Belva, S Henriet, E Van den Abbeel, et al.
Gastroenterologie Clinique Et Biologique
|
January 1, 1997
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]
C Bidaud, R Salomon, P Edery, et al.
Human Reproduction (Oxford, England)
|
November 26, 1999
Seven years of intracytoplasmic sperm injection and follow-up of 1987 subsequent children
M Bonduelle, M Camus, A De Vos, et al.
Human Reproduction (Oxford, England)
|
February 7, 2006
Paternal sperm concentration and growth and cognitive development in children born with a gestational age more than 32 weeks after assisted reproductive therapy
U-B Wennerholm, M Bonduelle, A Sutcliffe, et al.
Human Reproduction (Oxford, England)
|
July 15, 1998
Clinical experience with preimplantation genetic diagnosis and intracytoplasmic sperm injection
I Liebaers, K Sermon, C Staessen, et al.
Journal of Human Genetics
|
February 28, 2020
Preimplantation genetic testing with HLA matching: from counseling to birth and beyond
M De Rycke, A De Vos, F Belva, et al.
Nature Genetics
|
November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease
K Janssens, R Gershoni-Baruch, N Guañabens, et al.
Human Reproduction (Oxford, England)
|
September 1, 1996
The development of intracytoplasmic sperm injection
A Van Steirteghem, P Nagy, H Joris, et al.
Human Mutation
|
January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases
J Poncin, R Abs, B Velkeniers, et al.
Page
of 19
Search research articles
Search
Showing results (151-160 of 182) with videos related to
Sort By:
Page
of 19
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.
Human Reproduction (Oxford, England)
|
July 17, 2008
Neonatal outcome of 937 children born after transfer of cryopreserved embryos obtained by ICSI and IVF and comparison with outcome data of fresh ICSI and IVF cycles
F Belva, S Henriet, E Van den Abbeel, et al.
Gastroenterologie Clinique Et Biologique
|
January 1, 1997
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]
C Bidaud, R Salomon, P Edery, et al.
Human Reproduction (Oxford, England)
|
November 26, 1999
Seven years of intracytoplasmic sperm injection and follow-up of 1987 subsequent children
M Bonduelle, M Camus, A De Vos, et al.
Human Reproduction (Oxford, England)
|
February 7, 2006
Paternal sperm concentration and growth and cognitive development in children born with a gestational age more than 32 weeks after assisted reproductive therapy
U-B Wennerholm, M Bonduelle, A Sutcliffe, et al.
Human Reproduction (Oxford, England)
|
July 15, 1998
Clinical experience with preimplantation genetic diagnosis and intracytoplasmic sperm injection
I Liebaers, K Sermon, C Staessen, et al.
Journal of Human Genetics
|
February 28, 2020
Preimplantation genetic testing with HLA matching: from counseling to birth and beyond
M De Rycke, A De Vos, F Belva, et al.
Nature Genetics
|
November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease
K Janssens, R Gershoni-Baruch, N Guañabens, et al.
Human Reproduction (Oxford, England)
|
September 1, 1996
The development of intracytoplasmic sperm injection
A Van Steirteghem, P Nagy, H Joris, et al.
Human Mutation
|
January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases
J Poncin, R Abs, B Velkeniers, et al.
Page
of 19