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Publications by Jamila Ross
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
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