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Progress in Clinical and Biological Research
|
January 1, 1985
Turner's syndrome: updating on diagnosis and therapy
A De Paepe, M Matton
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Genetic counseling of a couple presenting respectively terminal transverse defects and congenital arthrogryposis
A De Paepe, S De Bie
International Journal of Pediatrics
|
February 13, 2013
Pharmacogenomics in children: advantages and challenges of next generation sequencing applications
O M Vanakker, A De Paepe
Journal of Medical Genetics
|
July 1, 1997
Marfan syndrome
A De Paepe, R C Hennekam
Journal of Medical Genetics
|
June 4, 1998
Psychosocial adaptation in adolescents and young adults with Marfan syndrome: an exploratory study
A Van Tongerloo, A De Paepe
Journal Belge De Radiologie
|
August 1, 1993
The osteoporosis pseudoglioma syndrome
J Capoen, A De Paepe, H Lauwers
Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie
|
April 13, 2007
Acquired chromosomal rearrangements targeting selected transcription factors: contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignancies
B Poppe, A De Paepe, F Speleman
Matrix Biology : Journal of the International Society for Matrix Biology
|
March 21, 1998
A four base pair insertion polymorphism in the 3' untranslated region of the COL1A1 gene is highly informative for null-allele testing in patients with osteogenesis imperfecta type I
L Nuytinck, C Coppin, A De Paepe
Prenatal Diagnosis
|
July 1, 1994
Why karyotype cystic hygroma cells?
M R Verschraegen-Spae, A De Paepe
Journal of Community Genetics
|
January 1, 2013
Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature
S Janssens, A De Paepe, P Borry
Page
of 18
Search research articles
Search
Showing results (11-20 of 173) with videos related to
Sort By:
Page
of 18
Progress in Clinical and Biological Research
|
January 1, 1985
Turner's syndrome: updating on diagnosis and therapy
A De Paepe, M Matton
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Genetic counseling of a couple presenting respectively terminal transverse defects and congenital arthrogryposis
A De Paepe, S De Bie
International Journal of Pediatrics
|
February 13, 2013
Pharmacogenomics in children: advantages and challenges of next generation sequencing applications
O M Vanakker, A De Paepe
Journal of Medical Genetics
|
July 1, 1997
Marfan syndrome
A De Paepe, R C Hennekam
Journal of Medical Genetics
|
June 4, 1998
Psychosocial adaptation in adolescents and young adults with Marfan syndrome: an exploratory study
A Van Tongerloo, A De Paepe
Journal Belge De Radiologie
|
August 1, 1993
The osteoporosis pseudoglioma syndrome
J Capoen, A De Paepe, H Lauwers
Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie
|
April 13, 2007
Acquired chromosomal rearrangements targeting selected transcription factors: contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignancies
B Poppe, A De Paepe, F Speleman
Matrix Biology : Journal of the International Society for Matrix Biology
|
March 21, 1998
A four base pair insertion polymorphism in the 3' untranslated region of the COL1A1 gene is highly informative for null-allele testing in patients with osteogenesis imperfecta type I
L Nuytinck, C Coppin, A De Paepe
Prenatal Diagnosis
|
July 1, 1994
Why karyotype cystic hygroma cells?
M R Verschraegen-Spae, A De Paepe
Journal of Community Genetics
|
January 1, 2013
Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature
S Janssens, A De Paepe, P Borry
Page
of 18