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F Erdogan

Showing results (31-40 of 37) with videos related to

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Cytogenetic and Genome Research|December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosisO Bartsch, Z Vlcková, F Erdogan, et al.
Journal of Endocrinological Investigation|April 9, 2002
Iodine status and goiter prevalence in Turkey before mandatory iodizationG Erdoğan, M F Erdogan, R Emral, et al.
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.
Human Molecular Genetics|January 4, 2001
X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applicationsR Sudbrak, G Wieczorek, U A Nuber, et al.
Journal of Endocrinological Investigation|December 24, 2005
Ret proto-oncogene mutations in apparently sporadic Turkish medullary thyroid carcinoma patients: Turkmen studyM F Erdogan, A Gürsoy, G Ozgen, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Cytogenetic and Genome Research|December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosisO Bartsch, Z Vlcková, F Erdogan, et al.
Journal of Endocrinological Investigation|April 9, 2002
Iodine status and goiter prevalence in Turkey before mandatory iodizationG Erdoğan, M F Erdogan, R Emral, et al.
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.
Human Molecular Genetics|January 4, 2001
X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applicationsR Sudbrak, G Wieczorek, U A Nuber, et al.
Journal of Endocrinological Investigation|December 24, 2005
Ret proto-oncogene mutations in apparently sporadic Turkish medullary thyroid carcinoma patients: Turkmen studyM F Erdogan, A Gürsoy, G Ozgen, et al.
Pageof 4