4.0 Article

High rates of de novo 15q11q13 inversions in human spermatozoa

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Genetics & Heredity

Inversion of the Williams Syndrome Region Is a Common Polymorphism Found More Frequently in Parents of Children With Williams Syndrome

Holly H. Hobart et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2010)

Review Medicine, Research & Experimental

Structural Variation in the Human Genome and its Role in Disease

Pawel Stankiewicz et al.

ANNUAL REVIEW OF MEDICINE (2010)

Article Cell Biology

Recurrent Inversion Events at 17q21.31 Microdeletion Locus Are Linked to the MAPT H2 Haplotype

P. N. Rao et al.

CYTOGENETIC AND GENOME RESEARCH (2010)

Article Developmental Biology

Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers

O. Molina et al.

MOLECULAR HUMAN REPRODUCTION (2010)

Review Genetics & Heredity

Copy Number Variation in Human Health, Disease, and Evolution

Feng Zhang et al.

ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS (2009)

Article Biochemistry & Molecular Biology

Characterization of six human disease-associated inversion polymorphisms

Francesca Antonacci et al.

HUMAN MOLECULAR GENETICS (2009)

Article Biochemistry & Molecular Biology

Copy number variation at the breakpoint region of isochromosome 17q

Claudia M. B. Carvalho et al.

GENOME RESEARCH (2008)

Review Obstetrics & Gynecology

Cytogenetic determinants of male fertility

R. H. Martin

HUMAN REPRODUCTION UPDATE (2008)

Article Genetics & Heredity

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Andrew J. Sharp et al.

NATURE GENETICS (2008)

Article Biotechnology & Applied Microbiology

Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23

H Sugawara et al.

GENOMICS (2003)

Article Genetics & Heredity

Mutational mechanisms of Williams-Beuren syndrome deletions

M Bayés et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)

Article Genetics & Heredity

Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14

P Ungaro et al.

JOURNAL OF MEDICAL GENETICS (2001)