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Publications by Lulu Meng

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

Frontiers in Genetics

Molecular Medicine

English

Related publications

Mutations in the FGFR2 Gene in Mexican Patients With Apert Syndrome

Genetics and Molecular Research

Molecular Biology

English

Presence of the Apert Canonical S252W FGFR2 Mutation in a Patient Without Severe Syndactyly.

Journal of Medical Genetics

English

Apert Syndrome: Clinical and Radiographic Features and Case Report

Revista Odonto Ciencia

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Hyaline Fibromatosis Syndrome With Mutation C.1074delT of the CMG2 Gene: A Case Report

Journal of Medical Case Reports

English

The Study of Abnormal Bone Development in the Apert Syndrome Fgfr2+/S252w Mouse Using a 3D Hydrogel Culture Model

English

Infantile-Onset Thiamine Responsive Megaloblastic Anemia Syndrome With SLC19A2 Mutation: A Case Report

Archivos Argentinos de Pediatria

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BCS1L Gene Mutation Causing GRACILE Syndrome: Case Report

Intensive Care Medicine

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A Case of Allgrove Syndrome With a Novel IVS7 +1 G>A Mutation of the AAAS Gene

Clinical Pediatric Endocrinology

English

Synchronous Bilateral Breast Carcinoma in a Patient With Cowden Syndrome With PTEN Mutation: A Case Report

Journal of Breast Disease

English