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R Ullmann

Showing results (61-70 of 67) with videos related to

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European Journal of Medical Genetics|November 14, 2007
Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephalyF Erdogan, J M Belloso, E Gabau, et al.
Cytogenetic and Genome Research|November 25, 2006
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardationF Erdogan, W Chen, M Kirchhoff, et al.
Journal of Medical Genetics|August 21, 2008
High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart diseaseF Erdogan, L A Larsen, L Zhang, et al.
International Journal of Andrology|November 29, 2007
Hypergonadotropic hypogonadism in a patient with inv ins (2;4)A Tzschach, C Ramel, A Kron, et al.
Molecular Psychiatry|March 24, 2010
Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigreeK-P Lesch, S Selch, T J Renner, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
European Journal of Medical Genetics|November 14, 2007
Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephalyF Erdogan, J M Belloso, E Gabau, et al.
Cytogenetic and Genome Research|November 25, 2006
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardationF Erdogan, W Chen, M Kirchhoff, et al.
Journal of Medical Genetics|August 21, 2008
High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart diseaseF Erdogan, L A Larsen, L Zhang, et al.
International Journal of Andrology|November 29, 2007
Hypergonadotropic hypogonadism in a patient with inv ins (2;4)A Tzschach, C Ramel, A Kron, et al.
Molecular Psychiatry|March 24, 2010
Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigreeK-P Lesch, S Selch, T J Renner, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 7