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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 neurofibromatosis
O Bartsch, Z Vlcková, F Erdogan, et al.
Journal of Endocrinological Investigation
|
April 9, 2002
Iodine status and goiter prevalence in Turkey before mandatory iodization
G 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 microcephaly
F 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 retardation
F 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 disease
F 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 applications
R 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 study
M F Erdogan, A Gürsoy, G Ozgen, et al.
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Search research articles
Search
Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 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 neurofibromatosis
O Bartsch, Z Vlcková, F Erdogan, et al.
Journal of Endocrinological Investigation
|
April 9, 2002
Iodine status and goiter prevalence in Turkey before mandatory iodization
G 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 microcephaly
F 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 retardation
F 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 disease
F 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 applications
R 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 study
M F Erdogan, A Gürsoy, G Ozgen, et al.
Page
of 4