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C Schrander-Stumpel

Showing results (1-10 of 41) with videos related to

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American Journal of Medical Genetics|November 24, 1999
Preconception care: challenge of the new millennium?C Schrander-Stumpel
European Journal of Pediatrics|June 13, 1998
Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counsellingC Schrander-Stumpel, J P Fryns
Journal of Mental Deficiency Research|June 1, 1991
The partial monosomy 10q syndrome: report on two patients and review of the developmental dataC Schrander-Stumpel, J P Fryns, G Hamers
American Journal of Medical Genetics|July 1, 1988
Caudal deficiency sequence in 7q terminal deletionC Schrander-Stumpel, J Schrander, J P Fryns, et al.
American Journal of Medical Genetics|July 15, 1992
A severe case of mandibuloacral dysplasia in a girlC Schrander-Stumpel, A Spaepen, J P Fryns, et al.
Clinical Genetics|August 1, 1995
Opitz BBBG syndrome: new family with late-onset, serious complicationJ Schrander, C Schrander-Stumpel, J Berg, et al.
Clinical Genetics|February 1, 1990
Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literatureC Schrander-Stumpel, J Schrander, J P Fryns, et al.
Journal of Medical Genetics|November 1, 1990
MASA syndrome: new clinical features and linkage analysis using DNA probesC Schrander-Stumpel, E Legius, J P Fryns, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Assignment of the aspartylglucosaminidase gene (AGA) to 4q33----q35 based on decreased activity in a girl with a 46,XX,del(4)(q33) karyotypeJ Engelen, A Hamers, C Schrander-Stumpel, et al.
American Journal of Medical Genetics|March 15, 1991
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneityC Schrander-Stumpel, J P Fryns, F A Beemer, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|November 24, 1999
Preconception care: challenge of the new millennium?C Schrander-Stumpel
European Journal of Pediatrics|June 13, 1998
Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counsellingC Schrander-Stumpel, J P Fryns
Journal of Mental Deficiency Research|June 1, 1991
The partial monosomy 10q syndrome: report on two patients and review of the developmental dataC Schrander-Stumpel, J P Fryns, G Hamers
American Journal of Medical Genetics|July 1, 1988
Caudal deficiency sequence in 7q terminal deletionC Schrander-Stumpel, J Schrander, J P Fryns, et al.
American Journal of Medical Genetics|July 15, 1992
A severe case of mandibuloacral dysplasia in a girlC Schrander-Stumpel, A Spaepen, J P Fryns, et al.
Clinical Genetics|August 1, 1995
Opitz BBBG syndrome: new family with late-onset, serious complicationJ Schrander, C Schrander-Stumpel, J Berg, et al.
Clinical Genetics|February 1, 1990
Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literatureC Schrander-Stumpel, J Schrander, J P Fryns, et al.
Journal of Medical Genetics|November 1, 1990
MASA syndrome: new clinical features and linkage analysis using DNA probesC Schrander-Stumpel, E Legius, J P Fryns, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Assignment of the aspartylglucosaminidase gene (AGA) to 4q33----q35 based on decreased activity in a girl with a 46,XX,del(4)(q33) karyotypeJ Engelen, A Hamers, C Schrander-Stumpel, et al.
American Journal of Medical Genetics|March 15, 1991
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneityC Schrander-Stumpel, J P Fryns, F A Beemer, et al.
Pageof 5