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Publications by Haoqing Zhang

Clinical and Genomic Evaluation of a Chinese Patient With a Novel Deletion Associated With Phelan–McDermid Syndrome

English

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China

Frontiers in Genetics

Molecular Medicine

English

Related publications

A 9-Year-Old-Girl With Phelan McDermid Syndrome, Who Had Been Diagnosed With an Autism Spectrum Disorder

Balkan Journal of Medical Genetics

English

Neural Selectivity for Communicative Auditory Signals in Phelan-McDermid Syndrome

Journal of Neurodevelopmental Disorders

Cognitive Neuroscience

Forensic Medicine

English

Functional Genomics Analysis of Phelan-McDermid Syndrome 22q13 Region During Human Neurodevelopment

Multidisciplinary

English

Cryptic 5q Deletion in a Patient With Myelodysplastic Syndrome

British Journal of Haematology

English

Acute Dystonia in a Patient With 22q11.2 Deletion Syndrome

English

Clinical Resistance Associated With a Novel MAP2K1 Mutation in a Patient With Langerhans Cell Histiocytosis

Pediatric Blood and Cancer

English

Identification of a Novel Deletion in UDP-glucuronosyltransferase Gene in a Patient With Crigler–Najjar Syndrome Type I

Blood Cells, Molecules, and Diseases

Molecular Medicine

Molecular Biology

English

A Novel Indicator of Lipid Accumulation Product Associated With Metabolic Syndrome in Chinese Children and Adolescents

Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy

Internal Medicine

English

Novel FUS Deletion in a Patient With Juvenile Amyotrophic Lateral Sclerosis

Archives of Neurology

English