Structural variants: changing the landscape of chromosomes and design of disease studies
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
[PDF][PDF] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle, SW Scherer - translocations, 2006 - gmo-qpcr-analysis.info
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
[PDF][PDF] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle… - …, 2006 - gene-quantification.com
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
[引用][C] Structural variants: changing the landscape of chromosomes and design of disease studies
L FEUK, CR MARSHALL, RF WINTLE… - Human molecular …, 2006 - pascal-francis.inist.fr
Structural variants : changing the landscape of chromosomes and design of disease studies
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
[PDF][PDF] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle, SW Scherer - translocations, 2006 - gene-quantification.eu
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
[引用][C] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle… - Human Molecular Genetics, 2006 - cir.nii.ac.jp
Structural variants: changing the landscape of chromosomes and design of disease studies |
CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 論文・データをさがす 大学 …
CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 論文・データをさがす 大学 …
[PDF][PDF] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle… - …, 2006 - gene-quantification.com
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle… - Human molecular …, 2006 - pubmed.ncbi.nlm.nih.gov
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
[PDF][PDF] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle, SW Scherer - translocations, 2006 - gene-quantification.de
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …
[PDF][PDF] Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle, SW Scherer - translocations, 2006 - gene-quantification.de
The near completeness of human chromosome sequences is facilitating accurate
characterization and assessment of all classes of genomic variation. Particularly, using the …
characterization and assessment of all classes of genomic variation. Particularly, using the …