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F A Beemer

Showing results (31-40 of 177) with videos related to

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Clinical Dysmorphology|July 1, 1996
Pili bifurcati: occurring in association with the mosaic trisomy 8 syndromeL J Breslau-Siderius, F A Beemer, B W Boom
Tijdschrift Voor Kindergeneeskunde|August 1, 1982
[A newborn infant with the xxxxy-syndrome]N Muis, B P Cats, P F Ippel, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 4, 1984
[Intrauterine death or infant death shortly after birth: reporting and diagnostic aspects]G C Christiaens, F A Beemer, H W Bruinse, et al.
Ophthalmic Paediatrics and Genetics|April 1, 1985
Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocationF A Beemer, M Duran, S K Wadman, et al.
International Journal of Oral and Maxillofacial Surgery|May 19, 2007
Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 geneR J J van Es, D Wittebol-Post, F A Beemer
European Journal of Neurology|July 25, 2000
Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxiasH J Schelhaas, P F Ippel, F A Beemer, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Leg duplication and kidney agenesis: case report and pathogenic considerationsP J Van Groesen, F A Beemer, J H Van de Kamp
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1977
Rapid enzymic micromethod for the quantitative determination of L(+)alanine in blood and urineR B Schutgens, C T Awie, F A Beemer, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported familiesM G Ausems, K ten Berg, F A Beemer, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
A patient with alpha-ketoadipic and alpha-aminoadipic aciduriaM Duran, F A Beemer, S K Wadman, et al.
Pageof 18

Showing results (31-40 of 177) with videos related to

Sort By:
Pageof 18
Clinical Dysmorphology|July 1, 1996
Pili bifurcati: occurring in association with the mosaic trisomy 8 syndromeL J Breslau-Siderius, F A Beemer, B W Boom
Tijdschrift Voor Kindergeneeskunde|August 1, 1982
[A newborn infant with the xxxxy-syndrome]N Muis, B P Cats, P F Ippel, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 4, 1984
[Intrauterine death or infant death shortly after birth: reporting and diagnostic aspects]G C Christiaens, F A Beemer, H W Bruinse, et al.
Ophthalmic Paediatrics and Genetics|April 1, 1985
Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocationF A Beemer, M Duran, S K Wadman, et al.
International Journal of Oral and Maxillofacial Surgery|May 19, 2007
Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 geneR J J van Es, D Wittebol-Post, F A Beemer
European Journal of Neurology|July 25, 2000
Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxiasH J Schelhaas, P F Ippel, F A Beemer, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Leg duplication and kidney agenesis: case report and pathogenic considerationsP J Van Groesen, F A Beemer, J H Van de Kamp
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1977
Rapid enzymic micromethod for the quantitative determination of L(+)alanine in blood and urineR B Schutgens, C T Awie, F A Beemer, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported familiesM G Ausems, K ten Berg, F A Beemer, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
A patient with alpha-ketoadipic and alpha-aminoadipic aciduriaM Duran, F A Beemer, S K Wadman, et al.
Pageof 18