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J-P Fryns

Showing results (121-130 of 787) with videos related to

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Genetic Counseling (Geneva, Switzerland)|February 12, 2002
Intrafamilial clinical variability in type C brachydactylyP Debeer, L De Smet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?C Maximilian, D M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndromeD M Ioan, C Maximilian, J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 23, 2012
A new syndrome: multiple congenital abnormalities and mental retardation in two brothersM Dundar, S Y Ozdemir, J P Fryns
American Journal of Medical Genetics|May 15, 1994
Regional Proteus syndrome and somatic mosaicismE Smeets, J P Fryns, M M Cohen
European Journal of Pediatrics|December 1, 1992
Deletion of the short arm of the X chromosome: a hereditary form of Turner syndromeG Massa, M Vanderschueren-Lodeweyckx, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Bilateral aplasia of the thumb, proximal radioulnar synostosis and unilateral synostosis of metacarpals 4 and 5Ph Debeer, L De Smet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosisL De Smet, K Keymolen, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Symbrachydactyly involving hands and feetL De Smet, G Fabry, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 23, 2005
De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literatureT Lukusa, J R Vermeesch, J P Fryns
Pageof 79

Showing results (121-130 of 787) with videos related to

Sort By:
Pageof 79
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
Intrafamilial clinical variability in type C brachydactylyP Debeer, L De Smet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?C Maximilian, D M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndromeD M Ioan, C Maximilian, J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 23, 2012
A new syndrome: multiple congenital abnormalities and mental retardation in two brothersM Dundar, S Y Ozdemir, J P Fryns
American Journal of Medical Genetics|May 15, 1994
Regional Proteus syndrome and somatic mosaicismE Smeets, J P Fryns, M M Cohen
European Journal of Pediatrics|December 1, 1992
Deletion of the short arm of the X chromosome: a hereditary form of Turner syndromeG Massa, M Vanderschueren-Lodeweyckx, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Bilateral aplasia of the thumb, proximal radioulnar synostosis and unilateral synostosis of metacarpals 4 and 5Ph Debeer, L De Smet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosisL De Smet, K Keymolen, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Symbrachydactyly involving hands and feetL De Smet, G Fabry, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 23, 2005
De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literatureT Lukusa, J R Vermeesch, J P Fryns
Pageof 79