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J-P Fryns

Showing results (21-30 of 1,120) with videos related to

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Genetic Counseling (Geneva, Switzerland)|October 24, 2000
Hypersplenism and portal hypertension with vena porta thrombosis in cartilage-hair hypoplasia (metaphyseal chondrodysplasia, McKusick type, MIM *250250)J P Fryns
Prenatal Diagnosis|January 1, 1995
Prenatal diagnosis and long survival of Fryns syndromeJ P Fryns
Journal of Medical Genetics|August 1, 1987
Congenital scalp defects with distal limb reduction anomaliesJ P Fryns
Archives Francaises De Pediatrie|May 1, 1988
[Unmanageable hair syndrome associated with epilepsy, deafness and phalangeal aplasia, or William's syndrome?]J P Fryns
Clinical Dysmorphology|August 5, 1998
Meier-Gorlin syndrome: the adult phenotypeJ P Fryns
Journal of Medical Genetics|July 25, 1998
Another holoprosencephaly locus at 7q21.2?J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 3, 2001
Micro-ablepharon of the upper eyelids and vaginal atresiaJ P Fryns
American Journal of Medical Genetics|April 24, 1999
On the nosology of severe acrofacial dysostosis with limb deficiencyJ P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Neuroblastoma in patients with constitutional chromosomal changesJ P Fryns
American Journal of Medical Genetics|January 1, 1993
Dolichomegasigmoid in Aarskog syndromeJ P Fryns
Pageof 112

Showing results (21-30 of 1,120) with videos related to

Sort By:
Pageof 112
Genetic Counseling (Geneva, Switzerland)|October 24, 2000
Hypersplenism and portal hypertension with vena porta thrombosis in cartilage-hair hypoplasia (metaphyseal chondrodysplasia, McKusick type, MIM *250250)J P Fryns
Prenatal Diagnosis|January 1, 1995
Prenatal diagnosis and long survival of Fryns syndromeJ P Fryns
Journal of Medical Genetics|August 1, 1987
Congenital scalp defects with distal limb reduction anomaliesJ P Fryns
Archives Francaises De Pediatrie|May 1, 1988
[Unmanageable hair syndrome associated with epilepsy, deafness and phalangeal aplasia, or William's syndrome?]J P Fryns
Clinical Dysmorphology|August 5, 1998
Meier-Gorlin syndrome: the adult phenotypeJ P Fryns
Journal of Medical Genetics|July 25, 1998
Another holoprosencephaly locus at 7q21.2?J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 3, 2001
Micro-ablepharon of the upper eyelids and vaginal atresiaJ P Fryns
American Journal of Medical Genetics|April 24, 1999
On the nosology of severe acrofacial dysostosis with limb deficiencyJ P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Neuroblastoma in patients with constitutional chromosomal changesJ P Fryns
American Journal of Medical Genetics|January 1, 1993
Dolichomegasigmoid in Aarskog syndromeJ P Fryns
Pageof 112