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J-P Fryns

Showing results (61-70 of 1,120) with videos related to

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Journal of Medical Genetics|July 1, 1988
Holoprosencephaly and postaxial polydactyly: another observationP Moerman, J P Fryns
American Journal of Medical Genetics|October 1, 1987
X-linked mental retardation with marfanoid habitusJ P Fryns, M Buttiens
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Hematometra and sudden death after status epilepticus in the adolescent female with Fryns syndromeM Dingens, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
On the nosology of van der Woude syndrome and popliteal pterygium syndrome: implications for genetic counselingJ P Fryns, K Devriendt
American Journal of Medical Genetics|May 5, 2001
Popliteal pterygium and multiple pterygium syndromesJ P Fryns, P Moerman
Journal of Medical Genetics|September 22, 2001
Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delayM Syrrou, J P Fryns
Clinical Genetics|May 1, 1993
Miller postaxial acrofacial dysostosis syndrome. Follow-up data of a family and confirmation of autosomal recessive inheritanceK Chrzanowska, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasiaJ P Fryns, P Moerman
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Normal/trisomy 13 mosaicism in a 38-year-old maleP Petit, J P Fryns
Journal De Genetique Humaine|September 1, 1989
[Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year]K Chrzanowska, J P Fryns
Pageof 112

Showing results (61-70 of 1,120) with videos related to

Sort By:
Pageof 112
Journal of Medical Genetics|July 1, 1988
Holoprosencephaly and postaxial polydactyly: another observationP Moerman, J P Fryns
American Journal of Medical Genetics|October 1, 1987
X-linked mental retardation with marfanoid habitusJ P Fryns, M Buttiens
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Hematometra and sudden death after status epilepticus in the adolescent female with Fryns syndromeM Dingens, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
On the nosology of van der Woude syndrome and popliteal pterygium syndrome: implications for genetic counselingJ P Fryns, K Devriendt
American Journal of Medical Genetics|May 5, 2001
Popliteal pterygium and multiple pterygium syndromesJ P Fryns, P Moerman
Journal of Medical Genetics|September 22, 2001
Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delayM Syrrou, J P Fryns
Clinical Genetics|May 1, 1993
Miller postaxial acrofacial dysostosis syndrome. Follow-up data of a family and confirmation of autosomal recessive inheritanceK Chrzanowska, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasiaJ P Fryns, P Moerman
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Normal/trisomy 13 mosaicism in a 38-year-old maleP Petit, J P Fryns
Journal De Genetique Humaine|September 1, 1989
[Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year]K Chrzanowska, J P Fryns
Pageof 112