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C T Schrander-Stumpel

Showing results (1-10 of 42) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|July 6, 2000
[Klinefelter syndrome in young children: possibility of diagnosis]N Boluyt, W W Hack, C T Schrander-Stumpel
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Opitz-C syndrome: on the nosology of mental retardation and trigonocephalyC Schaap, C T Schrander-Stumpel, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
X-linked mental retardation and neurological symptoms: a nosological approachC T Schrander-Stumpel, C J Höweler, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Congenital camptodactyly associated with the 48,XXYY syndromeA M Bosch, W W Hack, C T Schrander-Stumpel
Clinical Genetics|March 1, 1990
Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21))C T Schrander-Stumpel, J P Fryns, G G Hamers
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A patient with pituitary growth hormone deficiency and May-Hegglin anomaly: a distinct entity?W J Gerver, A V Neucker, C T Schrander-Stumpel
American Journal of Medical Genetics|December 26, 2001
Acampomelic campomelic syndromeU Moog, N J Jansen, G Scherer, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The lethal multiple pterygium syndrome: a nosological approachC E de Die-Smulders, C T Schrander-Stumpel, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Distal arthrogryposis, specific facial dysmorphism and psychomotor retardation: a recognizable entity in surviving patients with the fetal akinesia deformation sequenceC T Schrander-Stumpel, J P Fryns, J J Schrander, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Partial trisomy 15q: report of a patient and literature reviewK Chandler, C T Schrander-Stumpel, J Engelen, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Nederlands Tijdschrift Voor Geneeskunde|July 6, 2000
[Klinefelter syndrome in young children: possibility of diagnosis]N Boluyt, W W Hack, C T Schrander-Stumpel
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Opitz-C syndrome: on the nosology of mental retardation and trigonocephalyC Schaap, C T Schrander-Stumpel, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
X-linked mental retardation and neurological symptoms: a nosological approachC T Schrander-Stumpel, C J Höweler, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Congenital camptodactyly associated with the 48,XXYY syndromeA M Bosch, W W Hack, C T Schrander-Stumpel
Clinical Genetics|March 1, 1990
Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21))C T Schrander-Stumpel, J P Fryns, G G Hamers
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A patient with pituitary growth hormone deficiency and May-Hegglin anomaly: a distinct entity?W J Gerver, A V Neucker, C T Schrander-Stumpel
American Journal of Medical Genetics|December 26, 2001
Acampomelic campomelic syndromeU Moog, N J Jansen, G Scherer, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The lethal multiple pterygium syndrome: a nosological approachC E de Die-Smulders, C T Schrander-Stumpel, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Distal arthrogryposis, specific facial dysmorphism and psychomotor retardation: a recognizable entity in surviving patients with the fetal akinesia deformation sequenceC T Schrander-Stumpel, J P Fryns, J J Schrander, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Partial trisomy 15q: report of a patient and literature reviewK Chandler, C T Schrander-Stumpel, J Engelen, et al.
Pageof 5