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Chu Lee Wu

St Mary's Hospital

17

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660

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BRCA2: a cause of Li–Fraumeni-like syndrome

2007 Journal of Medical Genetics
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Coinheritance of two rare genodermatoses (Papillon–Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study

2004 British Journal of Dermatology
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Co-inheritance of two rare genodermatoses (Papillon Lefevre syndrome and Oculocutaneous Albinism Type 1) in two families

2004 British Journal of Dermatology
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Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas

2002 Journal of Medical Genetics
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Germline mutation of ARF in a melanoma kindred

2002 Human Molecular Genetics
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Re: Characterization of Hereditary Nonpolyposis Colorectal Cancer Families From a Population-Based Series of Cases

2001 Journal of the National Cancer Institute
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DNA studies underestimate the role of CDKN2A in oral squamous cell carcinoma (OSCC)

1999
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DNA studies underestimate the major role of CDKN2A inactivation in oral and oropharyngeal squamous cell carcinomas

1999 Genes, Chromosomes and Cancer
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Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas.

1998 Journal of Medical Genetics
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Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosis.

1998 American Journal of Human Genetics
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Citations (113)