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Genetic Counseling (Geneva, Switzerland)
|
February 12, 2002
Intrafamilial clinical variability in type C brachydactyly
P 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 syndrome
D 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 brothers
M Dundar, S Y Ozdemir, J P Fryns
American Journal of Medical Genetics
|
May 15, 1994
Regional Proteus syndrome and somatic mosaicism
E 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 syndrome
G 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 5
Ph 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 synostosis
L De Smet, K Keymolen, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 29, 1998
Symbrachydactyly involving hands and feet
L 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 literature
T Lukusa, J R Vermeesch, J P Fryns
Page
of 79
Search research articles
Search
Showing results (121-130 of 787) with videos related to
Sort By:
Page
of 79
Genetic Counseling (Geneva, Switzerland)
|
February 12, 2002
Intrafamilial clinical variability in type C brachydactyly
P 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 syndrome
D 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 brothers
M Dundar, S Y Ozdemir, J P Fryns
American Journal of Medical Genetics
|
May 15, 1994
Regional Proteus syndrome and somatic mosaicism
E 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 syndrome
G 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 5
Ph 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 synostosis
L De Smet, K Keymolen, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 29, 1998
Symbrachydactyly involving hands and feet
L 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 literature
T Lukusa, J R Vermeesch, J P Fryns
Page
of 79