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Publications by Elisabeth M. Froschauer

TheLETM1/YOL027Gene Family Encodes a Factor of the Mitochondrial K+Homeostasis With a Potential Role in the Wolf-Hirschhorn Syndrome

Journal of Biological Chemistry

Molecular Biology

English

Related publications

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

English

A Survey of Antiepileptic Drug Responses Identifies Drugs With Potential Efficacy for Seizure Control in Wolf–Hirschhorn Syndrome

Epilepsy and Behavior

Behavioral Neuroscience

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

Perioperative Care of an Infant With Wolf-Hirschhorn Syndrome: Is There a Risk of Malignant Hyperthermia

Journal of Medical Cases

English

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

Journal of Medical Genetics

English

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

Journal of Medical Genetics

English

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

European Journal of Human 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