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Publications by Andrew D Mumford

Clinical Features and Molecular Analysis of Seven British Kindreds With Hereditary Hyperferritinaemia Cataract Syndrome

European Journal of Human Genetics

English

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On the Hyperferritinemia and Hereditary Cataract Syndrome

Open Journal of Blood Diseases

English

Molecular Genetic Diagnosis and Clinical Features of Hereditary Neuropathy With Liability to Pressure Palsies

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Monitoring of Kindreds With Hereditary Predisposition for Cutaneous Melanoma and Dysplastic Nevus Syndrome: Results of a Swedish Preventive Program

Journal of Clinical Oncology

Cancer Research

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Clinical Features and Genetic Analysis of Korean Patients With Loeys–Dietz Syndrome

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Clinical and Molecular Features of Ewing Sarcoma in a Patient With Triple-X Syndrome

Cancer Genetics and Cytogenetics

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Clinical and Molecular Analysis of Nine Families With Adams–Oliver Syndrome

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Myeloproliferative Hypereosinophilic Syndrome: Retrospective Analysis of Cytogenetic and Molecular Features

Journal of Allergy and Clinical Immunology

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Hereditary Deficiencies of Complement Components. Examination, Frequency and Clinical Features.

SEIBUTSU BUTSURI KAGAKU

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Hereditary Spastic Paraplegia: Clinico-Pathologic Features and Emerging Molecular Mechanisms

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Forensic Medicine

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