Genetics Articles

Article Name

21 Hydroxylase Deficiency
5 Alpha Reductase Deficiency
A Review Of Hereditary Colorectal Cancers
Abciximab
Abetalipoproteinemia
Acanthocytosis
Acoustic Neuroma (Vestibular Schwannoma)
Acquired Angioedema
Acquired Digital Fibrokeratoma
Acrodermatitis Enteropathica
Acrokeratoelastoidosis
Acrokeratosis Verruciformis of Hopf
Actinic Prurigo
Actinomycosis
Acute Ankle Sprain
Acute Intermittent Porphyria
Acute Myocardial Infarction
Acute Retinal Necrosis
Aggression In Hypothalamic Hamartoma
Alagille Syndrome
Albinism
Allopurinol
Alpha 1 Antitrypsin Deficiency
Alpha 1 Antitrypsin Mutation
Alpha Fetoprotein (AFP, Maternal Serum Alpha Fetoprotein, MSAFP)
Alpha Thalassemia (Hemoglobin H Disease)
Alport Syndrome
Alzheimer Disease
Amiloride
Amniotic Fluid Index (AFI)
Amyloid Beta Peptide
Anatomy, Abdomen and Pelvis, Seminal Vesicle
Anatomy, Abdomen and Pelvis, Sigmoid Colon
Anatomy, Bony Pelvis and Lower Limb, Foot
Anatomy, Head and Neck, Eye Iris Sphincter Muscle
Anatomy, Head and Neck, Nasal Cavity
Anatomy, Head and Neck, Occipital Bone, Artery, Vein, and Nerve
Anatomy, Head and Neck, Retropharyngeal Space
Anatomy, Head and Neck, Tooth Eruption
Anatomy, Thorax, Heart Anomalous Left Coronary Artery
Androgen Insensitivity Syndrome
Angiodysplasia
Angioid Streaks (Knapp Streaks)
Angiokeratoma Circumscriptum
Aniridia
Apert Syndrome
Aplasia Cutis Congenita
Aplastic Anemia
Apoptosis
Arginase Deficiency (Argininemia)
Arnold Chiari Malformation
Arrhythmogenic Right Ventricular Cardiomyopathy
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atlantoaxial Instability
Atopy
Atrial Septal Defect (ASD)
Austin Flint Murmur
Autoimmune Myopathies (Dermatomyositis And Polymyositis)
Axenfeld Anomaly
Bacterial DNA Mutations
Bartter Syndrome
Basal Cell Carcinoma
Beevor Sign
Best Disease
Biochemistry, 5 Hydroxyindoleacetic Acid
Biochemistry, Apolipoprotein B
Biochemistry, Chylomicron
Biochemistry, Citric Acid Cycle
Biochemistry, DNA Replication
Biochemistry, DNA Structure
Biochemistry, Dopamine Receptors
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, HLA Antigens
Biochemistry, LDL Cholesterol
Biochemistry, Lipids
Biochemistry, Merosin
Biochemistry, Polymerase Chain Reaction (PCR)
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Biochemistry, Replication and Transcription
Biotin Deficiency
Birt Hogg Dube Syndrome
Blighted Ovum (Anembryonic Pregnancy)
Bloom Syndrome (Congenital Telangiectatic Erythema)
Blue Nevus
Bone Marrow Failure
Bone Marrow Transplantation In Sickle Cell Disease
Brachial Plexitis (Parsonage Turner Syndrome, Brachial Neuropathy, Brachial Radiculitis)
BRCA 1 and 2
Breast Magnetic Resonance Imaging (MRI)
Brugada Syndrome
Bruton Agammaglobulinemia
C 17 Hydroxylase Deficiency
C1 Esterase Inhibitor Deficiency
Calcifying Epithelioma of Malherbe
Canavan Disease
Cancer, Basal Cell
Cancer, Breast
Cancer, Burkitt Lymphoma
Cancer, Chemotherapy Acral Erythema (Palmar-Plantar Erythrodysesthesia, Palmoplantar Erythrodysesthesia, Hand-Foot Syndrome)
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Colon
Cancer, Endometrial
Cancer, Gastric
Cancer, Hodgkin Lymphoma
Cancer, Leukemia Cutis
Cancer, Lymphoplasmacytic Lymphoma (Waldenstrom Macroglobulinemia)
Cancer, Medulloblastoma
Cancer, Mesothelioma, Benign
Cancer, Neuroblastoma
Cancer, Ocular Melanoma
Cancer, Papillary Fibroelastoma
Cancer, Renal Cell
Cancer, Retinoblastoma
Cancer, Soft Tissue Clear Cell Sarcoma
Cancer, T Cell Prolymphocytic Leukemia
Cancer, Tumor-Suppressor Genes
Cardiac Fibroma
Carney Complex
Caroli Disease
Catheter Management Of Ventricular Septal Defect
Cavernous Venous Malformation
Cavum Septum Pellucidum
Celiac Disease
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Charcot Bouchard Aneurysm
Chediak Higashi Syndrome
Cherry Red Spot
Chest Trauma
Chest Wall Deformities
Child Syndrome
Choanal Atresia
Chorea
Chromosome Instability Syndromes
Chronic Diarrhea
Chronic Granulomatous Disease
Chronic Testicular Pain (Orchialgia)
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Lip
Coarctation of the Aorta
Cockayne Syndrome
Colchicine
Colon Resection
Color Vision
Congenital Adrenal Hyperplasia
Coronary Cameral Fistula
Cough
Cowden Disease (Multiple Hamartoma Syndrome)
Craniosynostosis
Creatine Phosphokinase
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crohn Disease
Crouzon Syndrome
Cutaneous Leiomyomas
Cutis Laxa (Elastolysis)
Cylindroma
Cystic Fibrosis
Cystic Fibrosis Related Diabetes (CFRD)
Dandy Walker Malformation
Danon Disease
Delayed Puberty
Dermatitis Herpetiformis
Dermatosis Papulosa Nigra
Diabetes, Maturity Onset in the Young (MODY)
Diamond Blackfan Anemia
DiGeorge Syndrome
Dowling Degos Disease
Down Syndrome (Trisomy 21)
Dubin Johnson Syndrome
Duchenne Muscular Dystrophy
Duodenal Atresia And Stenosis
Dyskeratosis Congenita
Dystonia
Dystonic Reactions
Dystrophinopathies
Ehlers Danlos Syndrome
Electrical Status Epilepticus In Sleep (ESES)
Embryology, Branchial Arches
Embryology, Central Nervous System, Malformations
Embryology, Ectoderm
Embryology, Epidermis
Embryology, Eye Malformations
Embryology, Kidney, Bladder, and Ureter
Embryology, Mullerian-inhibiting Factor
Embryology, Optic Cup
Embryology, Rectum and Anal Canal
Embryology, Uterus
EMS, Chest Injury
Epidermodysplasia Verruciformis
Epidermolytic Hyperkeratosis (Bullous Ichthyosiform Erythroderma)
Eptifibatide
Essential Thrombocytosis (Essential Thrombocythemia, ET)
Extramammary Paget Disease
Fabry Disease
Familial Adenomatous Polyposis
Familial Hyperlipidemia Type 1
Familial Hyperlipidemia Type 2a
Familial Hypocalciuric Hypercalcemia (FHH)
Fanconi Syndrome
Fatal Familial Insomnia
Female Development
Fetal Alcohol Syndrome
Fibrous Dysplasia
Fragile X Syndrome
Fructosamine
Fuchs Endothelial Dystrophy (FED)
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gardner Syndrome
Gastroesophageal Reflux Disease
Gaucher Disease
Generalized Pustular Psoriasis
Genetics, Autosomal Recessive
Genetics, DNA Damage and Repair
Genetics, DNA Packaging
Genetics, Epigenetic Mechanism
Genetics, Gonadal Dysgenesis
Genetics, Histocompatibility Antigen
Genetics, Histone Code
Genetics, Human Major Histocompatibility Complex (MHC)
Genetics, Meiosis
Genetics, Mitosis
Genetics, Nondisjunction
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Gitelman Syndrome
Glanzmann Thrombasthenia
Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I (Von Gierke Disease)
Glycogen Storage Disease Type II (Pompe Disease)
Good Samaritan Laws
Goodpasture Syndrome (Anti-glomerular Basement Membrane Antibody Disease)
Gorlin Syndrome (Basal Cell Nevus)
Gout (Podagra)
Gynecomastia
Hallervorden Spatz Disease (Pantothenate Kinase-Associated Neurodegeneration, PKAN)
Health Insurance Portability and Accountability Act (HIPAA)
Health Screening
Hearing Loss
Heart Failure And Ejection Fraction
Hemarthrosis
Hemiplegic Migraine
Hemochromatosis
Hemophilia
Hemophilia A
Hepatic (Hepatocellular) Adenoma
Hepatitis A
Hereditary Angioedema
Hereditary Spherocytosis
Hirsutism
Histology, Astrocytes
Histology, Myelin
Histology, Parathyroid Gland
Histology, Retina
Histology, Spermatogenesis
Histology, T-Cell Lymphocyte
HLA B27 Syndromes
Holt Oram Syndrome
Hurler Syndrome
Hydrocodone
Hyperbaric, Sensorineural Hearing Loss
Hypercalciuria
Hyperphosphatemia
Hyperpituitarism
Hypertonic Fluids
Hypertrichosis
Hypertrophic Cardiomyopathy
Hypertrophic Obstructive Cardiomyopathy
Hypomelanosis of Ito
Hypoparathyroidism
Hypospadias
Ichthyosis X-Linked
Idiopathic Guttate Hypomelanosis
IgA Nephropathy
Imatinib
Immunodeficiency
Impaired Bilirubin Conjugation
Imperforate Anus
Inborn Errors Of Metabolism
Infantile Cortical Hyperostosis (Caffey Disease)
Infantile Spasms
Influenza Vaccine
Informed Consent
Ingrown Toenails
Insulin Resistance
Insulinoma
Intellectual Disability
Interleukin
Iron Overload
Jervell and Lange Nielsen Syndrome
Job Syndrome (Hyperimmunoglobulin E)
Juvenile Xanthogranuloma (Nevoxanthoendothelioma, JXG)
Kallmann Syndrome
Kearns Sayre Syndrome
Keratosis Follicularis (Darier Disease)
Kidney Trauma
Klinefelter Syndrome
Klippel Feil Syndrome
Lafora Disease
Landau Kleffner Syndrome
Latex Allergy
Laugier-Hunziker Syndrome
Leber Optic Atrophy
Leukocyte Adhesion Deficiency
Li Fraumeni Syndrome
Liddle Syndrome
Lipodystrophies
Lipoma
Liver Function Tests
Loose Anagen Syndrome
Lymphoproliferative Disorders
Lynch Syndrome
Malabsorption Syndromes
Mallory Bodies
Marfan Syndrome
May Hegglin Anomaly
McCune Albright Syndrome
Medical Error Prevention
Medical Ethics
Melas Syndrome
Microcytic Hypochromic Anemia
Mitral Regurgitation
Mitral Valve Repair
Monilethrix
Moyamoya Disease
Muir-Torre Syndrome
Multiple Endocrine Neoplasia Type 1 (MEN I, Wermer Syndrome)
Multiple Endocrine Neoplasias, Type 2 (MEN II, Pheochromocytoma and Amyloid Producing Medullary Thyroid Carcinoma, Sipple Syndrome)
Multiple Sclerosis
Myelodysplastic Syndrome
Myeloperoxidase Deficiency
Myocardial Infarction
Neuroanatomy, Cranial Nerve 0 (Terminal Nerve)
Neuroanatomy, Lateral Corticospinal Tract
Neuroanatomy, Lower Motor Neuron Lesion
Neuroanatomy, Neurons
Neuroanatomy, Touch Receptor
Neurocutaneous Syndromes
Neurofibroma
Neurofibromatosis
Neurofibromatosis Type 1 (Von Recklinghausen)
Neurofibromatosis Type 2
Neuroma
Neuropathy
Nevus Comedonicus
Noonan Syndrome
Omphalocele
Open Angle Glaucoma
Ornithine Transcarbamylase Deficiency
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteochondroma
Osteogenesis Imperfecta
Paget Disease
Palmoplantar Psoriasis
Pancrelipase Therapy
Patau Syndrome
Pectus Carinatum (Pigeon Chest)
Pediatric Functional Constipation
Pediatric Hearing Loss
Pemphigus Vegetans
Pendred Syndrome
Penicillin Allergy
Pericholangitis
Pernio (Chilblains)
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Phenylketonuria
Phenytoin
Physiology, Adenosine Triphosphate (ATP)
Physiology, Adrenal Gland
Physiology, Antibody
Physiology, Brain
Physiology, Cardiovascular Murmurs
Physiology, Factor V
Physiology, Follicle Stimulating Hormone
Physiology, Gonadotropin Inhibitor
Physiology, Parathyroid
Physiology, Puberty
Physiology, Synuclein
Physiology, Thyroid
Physiology, Urea Cycle
Physiology, Vascular
Piebaldism
Piezogenic Pedal Papule
Pigmented Villonodular Synovitis
Pili Annulati
Poikiloderma Congenitale
Poland Syndrome
Polycystic Kidney Disease
Polycystic Kidney Disease Of Childhood
Polyglandular Autoimmune Syndrome, Type II (Carpenters, Schmidt)
Prader-Willi Syndrome
Precocious Puberty
Preconception Counseling
Pregnancy Medications
Prenatal Screening
Primary Hyperparathyroidism
Progeria (Werner Syndrome)
Prune Belly Syndrome
Pseudocholinesterase Deficiency
Pseudohypoparathyroidism
Pure Red Cell Aplasia
Raccoon Sign
Radiology, Image Production and Evaluation
Reactive Perforating Collagenosis
Recognizing Alcohol and Drug Impairment in the Workplace in Florida
Rectal Prolapse
Red Reflex
Reed Sternberg Cells
Renal Cyst
Renal Oncocytoma
Research Study
Restrictive (Infiltrative) Cardiomyopathy
Retinal Detachment
Retrognathia
Rett Syndrome
Reverse Transcriptase Inhibitors
Rhythm, QT Prolongation
Right Aortic Arches
Rinne Test
Rotor Syndrome
Sertoli-Cell-Only Syndrome
Severe Combined Immunodeficiency
Shwachman-Diamond Syndrome
Sickle Cell Anemia
Sickle Cell Trait
Sideroblastic Anemia
Splenic Sequestration Crisis
Splenic Trauma
Steatorrhea
Stevens Johnson Syndrome (Toxic Epidermal Necrolysis)
Succinylcholine Chloride
Sudden Cardiac Death
Supravalvar Aortic Stenosis (SVAS)
Sweat Testing
Sydenham Chorea
Syndromic Sensorineural Hearing Loss (SSHL)
Syringomyelia
Thalassemia
Thrombocytopenia
Thyroxine-Binding Globulin Deficiency
Tort
Tourette Syndrome And Other Tic Disorders
Tracheal Bronchus
Transposition Of The Great Arteries
Treadmill Stress Testing
Truncus Arteriosus
Tuberous Sclerosis
Tubular Adenoma
Turcot Syndrome
Ulcerative Colitis
Unconjugated Hyperbilirubinemia
Unconscious Patient
Urea Cycle Disorders
Velocardiofacial Syndrome
Villous Adenoma
Vismodegib
Vohwinkel Syndrome
Von Hippel Lindau Syndrome
Von Willebrand Disease
Western Blot (Protein Immunoblot)
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wilson Disease
Wiskott-Aldrich Syndrome
Wyburn-Mason Syndrome
Xeroderma Pigmentosum
X-linked Agammaglobulinemia
Young Syndrome
Zinc Deficiency