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J M Cobben

Showing results (31-40 of 63) with videos related to

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Clinical Genetics|February 1, 1992
A boy with Poland anomaly and facio-auriculo-vertebral dysplasiaJ M Cobben, A J van Essen, P C McParland, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletionH Scheffer, J M Cobben, R G Mensink, et al.
Human Genetics|November 1, 1995
A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysisG van der Steege, J M Cobben, J Osinga, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 25, 1995
[Multidisciplinary team treatment of children with a congenital disorders of the upper extremity]S Hiemstra, W H Eisma, J M Cobben, et al.
Lancet (London, England)|September 24, 1988
Prenatal diagnosis of cystic fibrosis where single affected child has diedG I te Meerman, L P ten Kate, J M Cobben, et al.
Neuromuscular Disorders : NMD|June 27, 2008
Survival in SMA type I: a prospective analysis of 34 consecutive casesJ M Cobben, H H Lemmink, I Snoeck, et al.
American Journal of Medical Genetics|August 1, 1989
Poland anomaly in mother and daughterJ M Cobben, P H Robinson, A J van Essen, et al.
Journal of Medical Genetics|May 1, 1995
Bilateral split hand/foot malformation and inv(7)(p22q21.3)J M Cobben, J B Verheij, W H Eisma, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 17, 2014
Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysisF A R Jansen, Y J Blumenfeld, A Fisher, et al.
Molecular Syndromology|May 10, 2012
Osteogenesis Imperfecta: A Review with Clinical ExamplesF S van Dijk, J M Cobben, A Kariminejad, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Clinical Genetics|February 1, 1992
A boy with Poland anomaly and facio-auriculo-vertebral dysplasiaJ M Cobben, A J van Essen, P C McParland, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletionH Scheffer, J M Cobben, R G Mensink, et al.
Human Genetics|November 1, 1995
A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysisG van der Steege, J M Cobben, J Osinga, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 25, 1995
[Multidisciplinary team treatment of children with a congenital disorders of the upper extremity]S Hiemstra, W H Eisma, J M Cobben, et al.
Lancet (London, England)|September 24, 1988
Prenatal diagnosis of cystic fibrosis where single affected child has diedG I te Meerman, L P ten Kate, J M Cobben, et al.
Neuromuscular Disorders : NMD|June 27, 2008
Survival in SMA type I: a prospective analysis of 34 consecutive casesJ M Cobben, H H Lemmink, I Snoeck, et al.
American Journal of Medical Genetics|August 1, 1989
Poland anomaly in mother and daughterJ M Cobben, P H Robinson, A J van Essen, et al.
Journal of Medical Genetics|May 1, 1995
Bilateral split hand/foot malformation and inv(7)(p22q21.3)J M Cobben, J B Verheij, W H Eisma, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 17, 2014
Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysisF A R Jansen, Y J Blumenfeld, A Fisher, et al.
Molecular Syndromology|May 10, 2012
Osteogenesis Imperfecta: A Review with Clinical ExamplesF S van Dijk, J M Cobben, A Kariminejad, et al.
Pageof 7