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J B Bijlsma

Showing results (21-30 of 38) with videos related to

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Brain : a Journal of Neurology|December 1, 1986
Myotonic dystrophy associated with hereditary motor and sensory neuropathyF Spaans, F G Jennekens, J F Mirandolle, et al.
Birth Defects Original Article Series|January 1, 1982
A possible new short rib syndrome in two sibsF A Beemer, J B Bijlsma, J Wladimiroff, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 18, 1987
[Clinical-genetic aspects, early diagnosis and neurosurgical treatment of familial intracranial aneurysms]J W ter Berg, J W Ludwig, J B Bijlsma, et al.
American Journal of Medical Genetics|November 1, 1992
Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: confirmation of the Gorlin-Chaudhry-Moss syndromeP F Ippel, R J Gorlin, W Lenz, et al.
European Journal of Pediatrics|June 1, 1988
Martsolf syndrome in a brother and sister: clinical features and pattern of inheritanceR C Hennekam, A G van de Meeberg, J M van Doorne, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial developmentM G Ausems, H G Van Spijker, H J Dijkhuis, et al.
Neuroradiology|January 1, 1987
Detection of unruptured familial intracranial aneurysms by intravenous digital subtraction angiography. Screening of two affected familiesJ W ter Berg, T M Overtoom, J W Ludwig, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1992
Encephalocraniocutaneous lipomatosis and oculocerebrocutaneous syndrome. A differential diagnostic problem?H E Loggers, J C Oosterwijk, W C Overweg-Plandsoen, et al.
European Journal of Pediatrics|July 17, 1998
Atelencephalic microcephaly: a case report and review of the literatureP F Ippel, E J Breslau-Siderius, W W Hack, et al.
Neurosurgery|September 1, 1988
Treatment of intact familial intracranial aneurysms: a decision-analytical approachH W ter Berg, D W Dippel, J D Habbema, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Brain : a Journal of Neurology|December 1, 1986
Myotonic dystrophy associated with hereditary motor and sensory neuropathyF Spaans, F G Jennekens, J F Mirandolle, et al.
Birth Defects Original Article Series|January 1, 1982
A possible new short rib syndrome in two sibsF A Beemer, J B Bijlsma, J Wladimiroff, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 18, 1987
[Clinical-genetic aspects, early diagnosis and neurosurgical treatment of familial intracranial aneurysms]J W ter Berg, J W Ludwig, J B Bijlsma, et al.
American Journal of Medical Genetics|November 1, 1992
Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: confirmation of the Gorlin-Chaudhry-Moss syndromeP F Ippel, R J Gorlin, W Lenz, et al.
European Journal of Pediatrics|June 1, 1988
Martsolf syndrome in a brother and sister: clinical features and pattern of inheritanceR C Hennekam, A G van de Meeberg, J M van Doorne, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial developmentM G Ausems, H G Van Spijker, H J Dijkhuis, et al.
Neuroradiology|January 1, 1987
Detection of unruptured familial intracranial aneurysms by intravenous digital subtraction angiography. Screening of two affected familiesJ W ter Berg, T M Overtoom, J W Ludwig, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1992
Encephalocraniocutaneous lipomatosis and oculocerebrocutaneous syndrome. A differential diagnostic problem?H E Loggers, J C Oosterwijk, W C Overweg-Plandsoen, et al.
European Journal of Pediatrics|July 17, 1998
Atelencephalic microcephaly: a case report and review of the literatureP F Ippel, E J Breslau-Siderius, W W Hack, et al.
Neurosurgery|September 1, 1988
Treatment of intact familial intracranial aneurysms: a decision-analytical approachH W ter Berg, D W Dippel, J D Habbema, et al.
Pageof 4