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Publications by P S Hart

Mutation in Kallikrein 4 Causes Autosomal Recessive Hypomaturation Amelogenesis Imperfecta

Journal of Medical Genetics

English

Identification of Cathepsin C Mutations in Ethnically Diverse Papillon-Lefevre Syndrome Patients

Journal of Medical Genetics

English

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Autosomal Dominant Amelogenesis Imperfecta Associated withENAMframeshift Mutation p.Asn36Ilefs56

Clinical Genetics

English

Enamelin and Autosomal-Dominant Amelogenesis Imperfecta

Critical Reviews in Oral Biology & Medicine

English

Identification of a Mutation Causing Deficient BMP1/mTLD Proteolytic Activity in Autosomal Recessive Osteogenesis Imperfecta

English

Amelogenesis Imperfecta

English

Amelogenesis Imperfecta

Oral Surgery, Oral Medicine, Oral Pathology

English

Amelogenesis Imperfecta and Screening of Mutation in Amelogenin Gene

Case Reports in Dentistry

English

Amelogenesis Imperfecta

English

Amelogenesis Imperfecta

Orphanet Journal of Rare Diseases

English

A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects

Molecular Biology

Cancer Research

English