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Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Corpus callosum agenesis in Coffin-Lowry syndrome
D Soekarman, J P Fryns
Journal of Medical Genetics
|
March 1, 1993
Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?
D Soekarman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome
D Soekarman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
On the nosology of the craniodigital syndromes: report of a family and review of the literature
D Soekarman, P Volcke, J P Fryns
Clinical Genetics
|
October 1, 1994
The KBG syndrome: follow-up data on three affected brothers
D Soekarman, P Volcke, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child
D Soekarman, J P Fryns, H van den Berghe
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Marden-Walker phenotype: a diagnostic dilemma
D Soekarman, P Volcke, E Legius, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome
D Soekarman, J P Fryns, P Casaer, et al.
Clinical Genetics
|
April 1, 1995
Variable expression of the popliteal pterygium syndrome in two 3-generation families
D Soekarman, J M Cobben, A Vogels, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1990
The Philadelphia translocation in CML and ALL: recent investigations, new detection methods
A Hagemeijer, D C van der Plas, D Soekarman, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Corpus callosum agenesis in Coffin-Lowry syndrome
D Soekarman, J P Fryns
Journal of Medical Genetics
|
March 1, 1993
Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?
D Soekarman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome
D Soekarman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
On the nosology of the craniodigital syndromes: report of a family and review of the literature
D Soekarman, P Volcke, J P Fryns
Clinical Genetics
|
October 1, 1994
The KBG syndrome: follow-up data on three affected brothers
D Soekarman, P Volcke, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child
D Soekarman, J P Fryns, H van den Berghe
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Marden-Walker phenotype: a diagnostic dilemma
D Soekarman, P Volcke, E Legius, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome
D Soekarman, J P Fryns, P Casaer, et al.
Clinical Genetics
|
April 1, 1995
Variable expression of the popliteal pterygium syndrome in two 3-generation families
D Soekarman, J M Cobben, A Vogels, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1990
The Philadelphia translocation in CML and ALL: recent investigations, new detection methods
A Hagemeijer, D C van der Plas, D Soekarman, et al.
Page
of 2