Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Qingmin Lin

De Novo Truncating Variant in NSD2gene Leading to Atypical Wolf-Hirschhorn Syndrome Phenotype

BMC Medical Genetics

English

Related publications

Paternal Origin of the De Novo Deleted Chromosome 4 in Wolf-Hirschhorn Syndrome.

Journal of Medical Genetics

English

WHSC1L1 (Wolf-Hirschhorn Syndrome Candidate 1 Like Gene 1)

Atlas of Genetics and Cytogenetics in Oncology and Haematology

Cancer Research

English

Genotype-Phenotype Correlation in 21 Patients With Wolf-Hirschhorn Syndrome Using High Resolution Array Comparative Genome Hybridisation (CGH)

Journal of Medical Genetics

English

Clinical Utility Gene Card For: Wolf–Hirschhorn (4p-) Syndrome

European Journal of Human Genetics

English

Molecular Characterisation of Chromosome 4p Deletions Resulting in Wolf-Hirschhorn Syndrome.

Journal of Medical Genetics

English

Growth Charts for Wolf-Hirschhorn Syndrome (0–4 Years of Age)

European Journal of Pediatrics

English

Meiotic Prophase I Defects in an Oligospermic Man With Wolf-Hirschhorn Syndrome With Ring Chromosome 4

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English

A Double Cryptic Chromosome Imbalance Is an Important Factor to Explain Phenotypic Variability in Wolf–Hirschhorn Syndrome

European Journal of Human Genetics

English

Experience of the Diagnosis and Observation of a Child With Wolf-Hirschhorn Syndrome

English