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Prenatal Diagnosis
|
November 14, 1997
Clinical application of preimplantation diagnosis for myotonic dystrophy
K Sermon, W Lissens, H Joris, et al.
Journal of Medical Genetics
|
May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR
W Lissens, S Desmyttere, M Bonduelle, et al.
Human Mutation
|
January 1, 1995
Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delT
B Mercier, W Lissens, M P Audrézet, et al.
Acta Neuropathologica
|
January 1, 1993
Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosis
A Michotte, L De Meirleir, W Lissens, et al.
Human Reproduction (Oxford, England)
|
December 1, 1996
Obstetric outcome of 904 pregnancies after intracytoplasmic sperm injection
A Wisanto, M Bonduelle, M Camus, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Lysosomal storage diseases presenting as transient or persistent hydrops fetalis
M Bonduelle, W Lissens, A Goossens, et al.
Human Reproduction (Oxford, England)
|
August 1, 1988
Oocyte donation in patients without ovarian function
P Devroey, A Wisanto, M Camus, et al.
Annales De Biologie Clinique
|
January 1, 1987
First trimester prenatal diagnosis of lysosomal storage disease. Study of alpha-L-fucosidase isoenzyme patterns in fetal and maternal tissue
W Lissens, T Bril, M Vercammen, et al.
Reproductive Biomedicine Online
|
April 13, 2005
HLA-matched embryos selected for siblings requiring haematopoietic stem cell transplantation: a psychological perspective
P Baetens, H Van de Velde, M Camus, et al.
Prenatal Diagnosis
|
August 1, 1991
Beta-glucuronidase activity in mouse oocytes, mouse preimplantation embryos, and human gametes
M Van Blerk, W Lissens, M Nijs, et al.
Page
of 22
Search research articles
Search
Showing results (111-120 of 211) with videos related to
Sort By:
Page
of 22
Prenatal Diagnosis
|
November 14, 1997
Clinical application of preimplantation diagnosis for myotonic dystrophy
K Sermon, W Lissens, H Joris, et al.
Journal of Medical Genetics
|
May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR
W Lissens, S Desmyttere, M Bonduelle, et al.
Human Mutation
|
January 1, 1995
Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delT
B Mercier, W Lissens, M P Audrézet, et al.
Acta Neuropathologica
|
January 1, 1993
Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosis
A Michotte, L De Meirleir, W Lissens, et al.
Human Reproduction (Oxford, England)
|
December 1, 1996
Obstetric outcome of 904 pregnancies after intracytoplasmic sperm injection
A Wisanto, M Bonduelle, M Camus, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Lysosomal storage diseases presenting as transient or persistent hydrops fetalis
M Bonduelle, W Lissens, A Goossens, et al.
Human Reproduction (Oxford, England)
|
August 1, 1988
Oocyte donation in patients without ovarian function
P Devroey, A Wisanto, M Camus, et al.
Annales De Biologie Clinique
|
January 1, 1987
First trimester prenatal diagnosis of lysosomal storage disease. Study of alpha-L-fucosidase isoenzyme patterns in fetal and maternal tissue
W Lissens, T Bril, M Vercammen, et al.
Reproductive Biomedicine Online
|
April 13, 2005
HLA-matched embryos selected for siblings requiring haematopoietic stem cell transplantation: a psychological perspective
P Baetens, H Van de Velde, M Camus, et al.
Prenatal Diagnosis
|
August 1, 1991
Beta-glucuronidase activity in mouse oocytes, mouse preimplantation embryos, and human gametes
M Van Blerk, W Lissens, M Nijs, et al.
Page
of 22