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Publications by M Alkan

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

Journal of Medical Genetics

English

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

BMC Medical Genetics

English

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

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

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

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

Atlas of Genetics and Cytogenetics in Oncology and Haematology

Cancer Research

English

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

European Journal of Human Genetics

English

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

European Journal of Human Genetics

English

Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome

American Journal of Human Genetics

English

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

English