Katherine L Lachlan

Katherine L Lachlan

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Katherine L Lachlan

Katherine L Lachlan

Publications by authors named "Katherine L Lachlan"

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10Publications

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PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature.

Am J Med Genet C Semin Med Genet 2019 Oct 14. Epub 2019 Oct 14.

Wessex Clinical Genetics Service, University Hospitals Southampton NHS Trust, Southampton, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.c.31743DOI Listing
October 2019

Cowden syndrome and the PTEN hamartoma tumor syndrome: how to define rare genetic syndromes.

J Natl Cancer Inst 2013 Nov 17;105(21):1595-7. Epub 2013 Oct 17.

Affiliations of author: Wessex Clinical Genetics Service, University of Southampton Foundation NHS Trust, Southampton, UK; and Academic Unit of Human Development and Health, Faculty of Medicine, University of Southampton, Southamption, UK.

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http://dx.doi.org/10.1093/jnci/djt290DOI Listing
November 2013

Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.

Eur J Hum Genet 2004 Oct;12(10):790-6

Wessex Clinical Genetics Service, Southampton University Hospitals NHS Trust, Southampton SO16 5YA, UK.

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http://dx.doi.org/10.1038/sj.ejhg.5201252DOI Listing
October 2004

Functional disomy resulting from duplications of distal Xq in four unrelated patients.

Hum Genet 2004 Oct 24;115(5):399-408. Epub 2004 Aug 24.

Wessex Clinical Genetics Service, Princess Anne Hospital, Coxford Road, SO16 5YA, Southampton, UK.

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http://dx.doi.org/10.1007/s00439-004-1175-xDOI Listing
October 2004