Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J-P Fryns

Showing results (101-110 of 1,120) with videos related to

Pageof 112
Sort By:
Annales De Genetique|January 1, 1996
Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patientJ P Fryns, G Hendrickx
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Early development (5 to 48 months) in Williams syndrome. A study of 14 childrenL Plissart, J P Fryns
American Journal of Medical Genetics|June 14, 1996
Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her childP Moerman, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Miller postaxial acrofacial dysostosis. The phenotypic changes with ageK Chrzanowska, J P Fryns
Annales De Genetique|January 1, 1984
Ring chromosome 21 in a normal femaleA Kleczkowska, J P Fryns
Clinical Genetics|July 1, 1984
Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome?J P Fryns, M Haspeslagh
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 28, 2004
Acro-osteolysis and symphalangism mutationsP Debeer, J-P Fryns
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndromeA Vogels, J P Fryns
Biochimica Et Biophysica Acta|December 15, 2007
Human chromosome fragilityT Lukusa, J P Fryns
American Journal of Medical Genetics|July 1, 1990
Mosaic normal/unbalanced karyotype and recurrent fetal wastageA Kleczkowska, J P Fryns
Pageof 112

Showing results (101-110 of 1,120) with videos related to

Sort By:
Pageof 112
Annales De Genetique|January 1, 1996
Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patientJ P Fryns, G Hendrickx
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Early development (5 to 48 months) in Williams syndrome. A study of 14 childrenL Plissart, J P Fryns
American Journal of Medical Genetics|June 14, 1996
Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her childP Moerman, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Miller postaxial acrofacial dysostosis. The phenotypic changes with ageK Chrzanowska, J P Fryns
Annales De Genetique|January 1, 1984
Ring chromosome 21 in a normal femaleA Kleczkowska, J P Fryns
Clinical Genetics|July 1, 1984
Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome?J P Fryns, M Haspeslagh
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 28, 2004
Acro-osteolysis and symphalangism mutationsP Debeer, J-P Fryns
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndromeA Vogels, J P Fryns
Biochimica Et Biophysica Acta|December 15, 2007
Human chromosome fragilityT Lukusa, J P Fryns
American Journal of Medical Genetics|July 1, 1990
Mosaic normal/unbalanced karyotype and recurrent fetal wastageA Kleczkowska, J P Fryns
Pageof 112