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Publications by Peter L. Geller

Molecular Confirmation of HRAS p.G12S in Siblings With Costello Syndrome

American Journal of Medical Genetics, Part A

English

Related publications

Neonatal Lethal Costello Syndrome and Unusual Dinucleotide Deletion/Insertion Mutations in HRAS Predicting p.Gly12Val

American Journal of Medical Genetics, Part A

English

HRAS Mutants Identified in Costello Syndrome Patients Can Induce Cellular Senescence: Possible Implications for the Pathogenesis of Costello Syndrome

Journal of Human Genetics

English

Fetal Costello Syndrome: A Description of the Phenotype of HRAS Exon 1 Mutations

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

English

Somatic HRAS p.G12S Mutation Causes Woolly Hair and Epidermal Nevi

Journal of Investigative Dermatology

Molecular Biology

English

Costello Syndrome: A Ras/Mitogen Activated Protein Kinase Pathway Syndrome (Rasopathy) Resulting From HRAS Germline Mutations

Genetics in Medicine

English

Costello Syndrome in Two Brazilian Children.

Journal of Medical Genetics

English

Female Siblings With Pendred's Syndrome.

Internal Medicine

Internal Medicine

English

Glaucoma in Siblings With Morquio Syndrome.

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English

MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn With Previously Unreported Clinical Features

Molecular Syndromology

English