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Publications by Willem Fennis
Concurrent Manifestation of Oligodontia and Thrombocytopenia Caused by a Contiguous Gene Deletion in 12p13.2: A Three‐generation Clinical Report
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Tooth Loss Prior to Radiation in Relation to Tumor Location in Patients With Head and Neck Cancer
International Journal of Prosthodontics
Medicine
Oral Surgery
Related publications
Smith-Magenis Syndrome: A New Contiguous Gene Syndrome. Report of Three New Cases.
Journal of Medical Genetics
Genetics
Clinical Manifestation of Hypercalcemia Caused by Adrenal Insufficiency in Hemodialysis Patients: A Case-Series Study
Internal Medicine
Internal Medicine
Medicine
Partial Manifestation of a Gene in Complete Three and Higher Point Backcross Data
Heredity
Genetics
Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Guyon's Canal Syndrome Caused by Schwannoma. A Report of Three Cases.
Orthopedics & Traumatology
Novel In-Frame FLNB Deletion Causes Larsen Syndrome in a Three-Generation Pedigree
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
Three Concurrent Prosthetic Joint Infections: A Case Report and Literature Review
International Journal of Musculoskeletal Disorders
A New Manifestation of Thrombocytopenia: Myocardial Haemorrhage With Symptomatic Arrhythmia
Journal of Clinical Pathology
Medicine
Forensic Medicine
Pathology
Vestibular Dysfunction Is a Manifestation of 22q11.2 Deletion Syndrome
American Journal of Medical Genetics, Part A
Genetics