4.1 Article

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Intragenic Deletions of IL1RAPL1: Report of Two Cases and Review of the Literature

Anne Behnecke et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)

Article Biochemistry & Molecular Biology

High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?

Laura Bernardini et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2010)

Article Biochemistry & Molecular Biology

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

Laura K. Conlin et al.

HUMAN MOLECULAR GENETICS (2010)

Article Genetics & Heredity

A de novo paradigm for mental retardation

Lisenka E. L. M. Vissers et al.

NATURE GENETICS (2010)

Review Genetics & Heredity

Cytogenetic contribution to uniparental disomy (UPD)

Thomas Liehr

MOLECULAR CYTOGENETICS (2010)

Editorial Material Biotechnology & Applied Microbiology

Isolated populations and complex disease gene identification

Kati Kristiansson et al.

GENOME BIOLOGY (2008)

Review Genetics & Heredity

Complex and segmental uniparental disomy updated

D. Kotzot

JOURNAL OF MEDICAL GENETICS (2008)

Review Multidisciplinary Sciences

A haplotype map of the human genome

D Altshuler et al.

NATURE (2005)

Article Genetics & Heredity

Detection of large-scale variation in the human genome

AJ Iafrate et al.

NATURE GENETICS (2004)