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S M Maas

Showing results (21-30 of 47) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|July 23, 1999
[Genes and genetics in Hirschsprung's disease]S M Maas, A S Brooks, R C Hennekam, et al.
Human Molecular Genetics|February 22, 2001
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWSJ Bliek, S M Maas, J M Ruijter, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|September 23, 2000
Intrauterine fetal death due to Farber disease: case reportG van Lijnschoten, J E Groener, S M Maas, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 19, 1992
[Pregnancy during residency]S M Maas, B W van 't Hoff, E H Rings, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 31, 2013
Influence of the 20-week anomaly scan on prenatal diagnosis and management of fetal facial cleftsS Ensing, C E Kleinrouweler, S M Maas, et al.
Pacing and Clinical Electrophysiology : PACE|December 1, 1990
Detection of ventricular tachycardia using scanning correlation analysisB M Steinhaus, R T Wells, S E Greenhut, et al.
Biochemical and Biophysical Research Communications|April 26, 1995
Further characterization of the 5'-flanking region of the rat lactase-phlorizin hydrolase geneM Verhave, S D Krasinski, S M Maas, et al.
European Journal of Medical Genetics|September 9, 2009
Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsJ Bliek, S Snijder, S M Maas, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 1, 2023
Genetic mutations and phenotype characteristics in peripheral vascular malformations: A systematic reviewM L E Stor, S E R Horbach, M M Lokhorst, et al.
Journal of Medical Genetics|July 10, 2009
Phenotype and genotype in 17 patients with Goltz-Gorlin syndromeS M Maas, M P Lombardi, A J van Essen, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Nederlands Tijdschrift Voor Geneeskunde|July 23, 1999
[Genes and genetics in Hirschsprung's disease]S M Maas, A S Brooks, R C Hennekam, et al.
Human Molecular Genetics|February 22, 2001
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWSJ Bliek, S M Maas, J M Ruijter, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|September 23, 2000
Intrauterine fetal death due to Farber disease: case reportG van Lijnschoten, J E Groener, S M Maas, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 19, 1992
[Pregnancy during residency]S M Maas, B W van 't Hoff, E H Rings, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 31, 2013
Influence of the 20-week anomaly scan on prenatal diagnosis and management of fetal facial cleftsS Ensing, C E Kleinrouweler, S M Maas, et al.
Pacing and Clinical Electrophysiology : PACE|December 1, 1990
Detection of ventricular tachycardia using scanning correlation analysisB M Steinhaus, R T Wells, S E Greenhut, et al.
Biochemical and Biophysical Research Communications|April 26, 1995
Further characterization of the 5'-flanking region of the rat lactase-phlorizin hydrolase geneM Verhave, S D Krasinski, S M Maas, et al.
European Journal of Medical Genetics|September 9, 2009
Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsJ Bliek, S Snijder, S M Maas, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 1, 2023
Genetic mutations and phenotype characteristics in peripheral vascular malformations: A systematic reviewM L E Stor, S E R Horbach, M M Lokhorst, et al.
Journal of Medical Genetics|July 10, 2009
Phenotype and genotype in 17 patients with Goltz-Gorlin syndromeS M Maas, M P Lombardi, A J van Essen, et al.
Pageof 5