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J B Bijlsma

Showing results (11-20 of 38) with videos related to

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European Journal of Pediatrics|October 1, 1981
Partial monosomy 10p syndromeJ M Klep-de Pater, J B Bijlsma, F M Alkema
Nederlands Tijdschrift Voor Geneeskunde|April 13, 1985
[Faciodigitogenital syndrome (Aarskog's syndrome)]C T Schrander-Stumpel, L H van Benthem, J B Bijlsma
Brain & Development|January 1, 1988
Megalencephaly: definition and classificationR H Gooskens, J Willemse, J B Bijlsma, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
MCA/MR syndrome in two female siblings: new entity or variant examples of Coffin-Lowry versus Atkin-Flaitz syndromes?A Jans, E F Ippel, P F Dijkstra, et al.
Journal of Child Neurology|November 1, 1995
Genetic heterogeneity of hereditary motor and sensory neuropathy type VIE F Ippel, D Wittebol-Post, F G Jennekens, et al.
Journal of Medical Genetics|June 1, 1985
Interstitial deletion of the long arm of chromosome 11J M Klep-de Pater, H F de France, J B Bijlsma
Ophthalmic Genetics|September 1, 1994
Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation. A new autosomal recessive disorder?P F Ippel, D Wittebol-Post, B P van Nesselrooij, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Interstitial deletion 11q. Case report and review of the literatureJ M De Pater, P F Ippel, J B Bijlsma, et al.
Tijdschrift Voor Kindergeneeskunde|June 1, 1981
Pure gonadal dysgenesis in a triple-x femaleL H van Benthem, J B Bijlsma, H A Delemarre-van de Waal
Human Genetics|January 19, 1978
Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndromeJ B Bijlsma, H F de France, L M Bleeker-Wagemakers, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
European Journal of Pediatrics|October 1, 1981
Partial monosomy 10p syndromeJ M Klep-de Pater, J B Bijlsma, F M Alkema
Nederlands Tijdschrift Voor Geneeskunde|April 13, 1985
[Faciodigitogenital syndrome (Aarskog's syndrome)]C T Schrander-Stumpel, L H van Benthem, J B Bijlsma
Brain & Development|January 1, 1988
Megalencephaly: definition and classificationR H Gooskens, J Willemse, J B Bijlsma, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
MCA/MR syndrome in two female siblings: new entity or variant examples of Coffin-Lowry versus Atkin-Flaitz syndromes?A Jans, E F Ippel, P F Dijkstra, et al.
Journal of Child Neurology|November 1, 1995
Genetic heterogeneity of hereditary motor and sensory neuropathy type VIE F Ippel, D Wittebol-Post, F G Jennekens, et al.
Journal of Medical Genetics|June 1, 1985
Interstitial deletion of the long arm of chromosome 11J M Klep-de Pater, H F de France, J B Bijlsma
Ophthalmic Genetics|September 1, 1994
Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation. A new autosomal recessive disorder?P F Ippel, D Wittebol-Post, B P van Nesselrooij, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Interstitial deletion 11q. Case report and review of the literatureJ M De Pater, P F Ippel, J B Bijlsma, et al.
Tijdschrift Voor Kindergeneeskunde|June 1, 1981
Pure gonadal dysgenesis in a triple-x femaleL H van Benthem, J B Bijlsma, H A Delemarre-van de Waal
Human Genetics|January 19, 1978
Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndromeJ B Bijlsma, H F de France, L M Bleeker-Wagemakers, et al.
Pageof 4