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Publications by Marijn Créton

Concurrent Manifestation of Oligodontia and Thrombocytopenia Caused by a Contiguous Gene Deletion in 12p13.2: A Three‐generation Clinical Report

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Related publications

Smith-Magenis Syndrome: A New Contiguous Gene Syndrome. Report of Three New Cases.

Journal of Medical Genetics
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Internal Medicine
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Partial Manifestation of a Gene in Complete Three and Higher Point Backcross Data

Heredity
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1957English

Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene

Neuromuscular Disorders
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2019English

Guyon's Canal Syndrome Caused by Schwannoma. A Report of Three Cases.

Orthopedics & Traumatology
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Novel In-Frame FLNB Deletion Causes Larsen Syndrome in a Three-Generation Pedigree

Cold Spring Harbor molecular case studies
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Three Concurrent Prosthetic Joint Infections: A Case Report and Literature Review

International Journal of Musculoskeletal Disorders
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A New Manifestation of Thrombocytopenia: Myocardial Haemorrhage With Symptomatic Arrhythmia

Journal of Clinical Pathology
MedicineForensic MedicinePathology
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Vestibular Dysfunction Is a Manifestation of 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A
Genetics
2019English

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