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J-P Fryns

Showing results (91-100 of 1,120) with videos related to

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American Journal of Medical Genetics|November 1, 1986
Distal osteolysis, short stature, mental retardation, and characteristic facial appearance: delineation of an autosomal recessive subtype of essential osteolysisP Petit, J P Fryns
Clinical Genetics|January 1, 1987
Population cytogenetics of autosomal fragile sitesJ P Fryns, P Petit
American Journal of Medical Genetics|May 1, 1991
New lethal acrofacial dysostosis syndromeJ P Fryns, A Kleckowska
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Prenatal diagnosis of central nervous system abnormalities: diagnostic possibilities and limitations of fetal neurosonographyI Witters, J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
Goeminne syndrome (OMIM 314300): another male patient 30 years laterJ P Fryns, D Gevers
Annales De Genetique|June 1, 1979
Interstital deletion of 13q associated with retinoblastoma and congenital malformationsP Petit, J P Fryns
Annales De Genetique|January 1, 1987
Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11)J P Fryns, A Kleczkowska
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The fetal akinesia deformation sequence. A fetopathological approachP Moerman, J P Fryns
Journal De Genetique Humaine|September 1, 1985
[Lethal skeletal dysplasias: delineation of a new distinct entity with spondylocostal dysostosis, multiple internal abnormalities and Dandy-Walker cyst]J P Fryns, P Moerman
American Journal of Medical Genetics|November 1, 1993
46,XY/46,XX mosaicism and congenital pulmonary lymphangiectasis with chylothoraxJ P Fryns, P Moerman
Pageof 112

Showing results (91-100 of 1,120) with videos related to

Sort By:
Pageof 112
American Journal of Medical Genetics|November 1, 1986
Distal osteolysis, short stature, mental retardation, and characteristic facial appearance: delineation of an autosomal recessive subtype of essential osteolysisP Petit, J P Fryns
Clinical Genetics|January 1, 1987
Population cytogenetics of autosomal fragile sitesJ P Fryns, P Petit
American Journal of Medical Genetics|May 1, 1991
New lethal acrofacial dysostosis syndromeJ P Fryns, A Kleckowska
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Prenatal diagnosis of central nervous system abnormalities: diagnostic possibilities and limitations of fetal neurosonographyI Witters, J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
Goeminne syndrome (OMIM 314300): another male patient 30 years laterJ P Fryns, D Gevers
Annales De Genetique|June 1, 1979
Interstital deletion of 13q associated with retinoblastoma and congenital malformationsP Petit, J P Fryns
Annales De Genetique|January 1, 1987
Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11)J P Fryns, A Kleczkowska
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The fetal akinesia deformation sequence. A fetopathological approachP Moerman, J P Fryns
Journal De Genetique Humaine|September 1, 1985
[Lethal skeletal dysplasias: delineation of a new distinct entity with spondylocostal dysostosis, multiple internal abnormalities and Dandy-Walker cyst]J P Fryns, P Moerman
American Journal of Medical Genetics|November 1, 1993
46,XY/46,XX mosaicism and congenital pulmonary lymphangiectasis with chylothoraxJ P Fryns, P Moerman
Pageof 112