Concepedia

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

David Monk, Louise Bentley, Megan P. Hitchins, Rachael Myler, Jill Clayton‐Smith, Samira Ismail, Sue Price, Michael Preece, Philip Stanier, Gudrun Moore

Human Genetics · 2002 · 91 citations · 36 references

DOI

Concepts

References

36

Differential activity of maternally and paternally derived chromosome regions in mice

B.M. Cattanach, Maggie Kirk · Nature · 1985 · 704 citations

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Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis et al. · American Journal of Medical Genetics · 1989 · 583 citations

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The HUGO Gene Nomenclature Committee (HGNC)

Sue Povey, Ruth C. Lovering, Elspeth A. Bruford et al. · Human Genetics · 2001 · 527 citations

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Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

James S. Sutcliffe, Mitsuyoshi Nakao, Susan L. Christian et al. · Nature Genetics · 1994 · 422 citations

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Charcot–Marie–Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

Carol A. Wise, A. Craig Chinault, Pragna I. Patel et al. · Nature Genetics · 1992 · 388 citations

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