Genetics-Medical Student Articles

Article Name

21 Hydroxylase Deficiency
A Review Of Hereditary Colorectal Cancers
Abciximab
Abetalipoproteinemia
Acanthocytosis
Acoustic Neuroma (Vestibular Schwannoma)
Acquired Angioedema
Acrokeratoelastoidosis
Acrokeratosis Verruciformis of Hopf
Actinic Keratosis
Acute Intermittent Porphyria
Aflatoxin Toxicity
Albinism
Alpers-Huttenlocher Syndrome (AHS, Alper Disease)
Alpha 1 Antitrypsin Deficiency
Alpha 1 Antitrypsin Mutation
Alpha Fetoprotein (AFP, Maternal Serum Alpha Fetoprotein, MSAFP)
Alport Syndrome
Ambiguous Genitalia And Disorders of Sexual Differentiation
Amniotic Fluid Index (AFI)
Amyloid Beta Peptide
Amyotrophic Lateral Sclerosis
Anatomy, Abdomen and Pelvis, Bowman Capsule
Anatomy, Abdomen and Pelvis, Seminal Vesicle
Anatomy, Abdomen and Pelvis, Sigmoid Colon
Anatomy, Head and Neck, Eye Iris Sphincter Muscle
Anatomy, Head and Neck, Parathyroid, Ectopic Glands
Anatomy, Head and Neck, Tooth Eruption
Androgen Insensitivity Syndrome
Angioid Streaks (Knapp Streaks)
Anhidrosis
Aniridia
Ankylosing Spondylitis
Anosmia
Aortic Insufficiency
Aortic Regurgitation
Aplastic Anemia
Apoptosis
Arginase Deficiency (Argininemia)
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atrioventricular Canal Defects
Autism Spectrum Disorder (Regressive Autism, Child Disintegrative Disorder)
Bacterial DNA Mutations
BAX Gene
Becker Muscular Dystrophy
Bernard Soulier Syndrome
Bicuspid Aortic Valve
Biochemistry, Apolipoprotein B
Biochemistry, Biliverdin
Biochemistry, Ceruloplasmin
Biochemistry, Chloride Channels
Biochemistry, Dihydrotestosterone
Biochemistry, DNA Replication
Biochemistry, DNA Structure
Biochemistry, Dopamine Receptors
Biochemistry, Essential Amino Acids
Biochemistry, Glycogen
Biochemistry, Glycogenolysis
Biochemistry, HLA Antigens
Biochemistry, Immunoglobulin A (IgA)
Biochemistry, Immunoglobulin M (IgM)
Biochemistry, Iron Absorption
Biochemistry, LDL Cholesterol
Biochemistry, Lipids
Biochemistry, Lipoprotein Lipase
Biochemistry, Low Density Lipoprotein
Biochemistry, Melanin
Biochemistry, Merosin
Biochemistry, Presenilin
Biochemistry, Protein Catabolism
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Biochemistry, Replication and Transcription
Biochemistry, Superoxides
Biochemistry, Tertiary Structure, Protein
Biochemistry, Tetrahydrofolate
Biochemstry, Fatty Acid Oxidation
Biotin Deficiency
Bleomycin
Bloom Syndrome (Congenital Telangiectatic Erythema)
Bone Marrow Failure
BRCA 1 and 2
Breast Cancer
Brown Sequard Syndrome
Brugada Syndrome
Bruton Agammaglobulinemia
C 17 Hydroxylase Deficiency
C1 Esterase Inhibitor Deficiency
Cafe Au Lait Macules
Cancer, Anorexia and Cachexia
Cancer, Burkitt Lymphoma
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Colon
Cancer, Lung Small Cell (Oat Cell)
Cancer, Neuroblastoma
Cancer, Osteosarcoma
Cancer, Renal Cell
Cancer, Retinoblastoma
Cancer, Tumor-Suppressor Genes
Cardiac Disease In Pregnancy
Carney Complex
Caroli Disease
Cavum Septum Pellucidum
Cerebral Amyloid Angiopathy
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Chediak Higashi Syndrome
Cherry Red Spot
Chest Wall Deformities
Cholinesterase Inhibitors
Chorea
Chromosome Instability Syndromes
Chronic Diarrhea
Chronic Granulomatous Disease
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Hand (Ectrodactyly, Split Hand)
Coarctation of the Aorta
Color Vision
Congenital Diaphragmatic Hernia
Cooley Anemia
Corneal Graft Rejection
Cough
Craniopharyngioma
Creatine Phosphokinase
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crohn Disease
Crouzon Syndrome
Cutis Verticis Gyrata
Cyanotic Heart Disease
Cyclic Neutropenia
Cystic Fibrosis
Cystic Fibrosis And Liver Disease
Dandy Walker Malformation
Danon Disease
Delayed Puberty
Dermatosis Papulosa Nigra
Development Milestones
Dextrocardia
Diamond Blackfan Anemia
DiGeorge Syndrome
Dowling Degos Disease
Down Syndrome (Trisomy 21)
Dubin Johnson Syndrome
Duchenne Muscular Dystrophy
Duodenal Atresia And Stenosis
Dyskeratosis Congenita
Ehlers Danlos Syndrome
Electrical Status Epilepticus In Sleep (ESES)
Embryology, Amniotic Fluid
Embryology, Central Nervous System
Embryology, Ectoderm
Embryology, Esophagus
Embryology, Eye
Embryology, Eye Malformations
Embryology, Kidney, Bladder, and Ureter
Embryology, Midgut
Embryology, Neural Tube
Embryology, Optic Cup
Embryology, Optic Fissure
Embryology, Pharyngeal Pouch
Embryology, Rectum and Anal Canal
Embryology, Sexual Development
Embryology, Week 2-3
Epidermolytic Hyperkeratosis (Bullous Ichthyosiform Erythroderma)
Fabry Disease
Factor V Leiden Deficiency
Familial Adenomatous Polyposis
Familial Hypercholesterolemia
Familial Hyperlipidemia Type 1
Familial Hyperlipidemia Type 2a
Familial Hypocalciuric Hypercalcemia (FHH)
Fanconi Syndrome
Female Development
Fetal Alcohol Syndrome
Fibrous Dysplasia
Fifth-Toe Deformities
Fragile X Syndrome
Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance)
GABA Receptor
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gardner Syndrome
Gaucher Disease
Genetics, Autosomal Dominant
Genetics, Autosomal Recessive
Genetics, Chromosome Abnormalities
Genetics, Chromosomes
Genetics, DNA Damage and Repair
Genetics, DNA Packaging
Genetics, Epigenetic Mechanism
Genetics, Female Gametogenesis
Genetics, Gonadal Dysgenesis
Genetics, Histocompatibility Antigen
Genetics, Histone Code
Genetics, Human Major Histocompatibility Complex (MHC)
Genetics, Meiosis
Genetics, Mitosis
Genetics, Nondisjunction
Genetics, Somatic Mutation
Genetics, Transposons
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Genetics, X-Linked Inheritance
Gilbert Syndrome
Gitelman Syndrome
Glanzmann Thrombasthenia
Gliomas
Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I (Von Gierke Disease)
Glycogen Storage Disease Type II (Pompe Disease)
Gout (Podagra)
Gower Sign
Gynecomastia
Health Screening
Hearing Loss
Hemiplegic Migraine
Hemochromatosis
Hemolytic Diseases Of The Newborn
Hemophilia
Hemophilia A
Hepatic Hemangioma
Hepatitis A
Hepatitis B
HER2
Hereditary Angioedema
Hereditary Spherocytosis
Histology, Cell
Histology, Cell Death
Histology, Leydig Cells
Histology, M Cell
Histology, Myelin
Histology, Parathyroid Gland
Histology, Plasma Cells
Histology, Spermatogenesis
Histology, T-Cell Lymphocyte
Hodgkin Lymphoma
Hurler Syndrome
Hypercholesterolemia
Hyperhomocysteinemia
Hypertrichosis
Hypertrophic Cardiomyopathy
Hypophosphatemia
Ichthyosis X-Linked
Imatinib
Impaired Bilirubin Conjugation
Inborn Errors Of Metabolism
Insulin Resistance
Intellectual Disability
Iron Overload
Jacobs (XYY) Syndrome
Jervell and Lange Nielsen Syndrome
Job Syndrome (Hyperimmunoglobulin E)
Kallmann Syndrome
Kayser-Fleischer Ring
Klinefelter Syndrome
Lafora Disease
Latent Autoimmune Diabetes
Leber Optic Atrophy
Lesch Nyhan Syndrome
Leukocyte Adhesion Deficiency
Li-Fraumeni Syndrome
Lipemia Retinalis
Lisch Nodules
Lymphangioma
Lynch Syndrome
Malabsorption Syndromes
Mallory Bodies
Maple Syrup Urine Disease
Marfan Syndrome
May Hegglin Anomaly
McCune Albright Syndrome
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
Myoclonic Epilepsy and Ragged Red Fibers (MERF)
Myotonic Dystrophy
Neuroanatomy, Corticobulbar Tract
Neuroanatomy, Cranial Nerve 7 (Facial)
Neuroanatomy, Dentate Nucleus
Neuroanatomy, Neural Crest
Neuroanatomy, Nucleus Caudate
Neurocutaneous Syndromes
Neurofibroma
Neurofibromatosis
Neurofibromatosis Type 1 (Von Recklinghausen)
Neurofibromatosis Type 2
Neuroma
Niemann-Pick Disease
Noonan Syndrome
Omphalocele
Optic Nerve Glioma
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteogenesis Imperfecta
Osteopetrosis
Paget Disease
Pancrelipase Therapy
Patau Syndrome
Pendred Syndrome
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Phenylketonuria
Photopic Vision
Physiology, Adenosine Triphosphate (ATP)
Physiology, Bile
Physiology, Brain
Physiology, Cardiovascular Murmurs
Physiology, Cellular Receptor
Physiology, Chorionic Gonadotropin
Physiology, Connective Tissue
Physiology, Follicle Stimulating Hormone
Physiology, Gluconeogenesis
Physiology, Krebs Cycle
Physiology, Leukotrienes
Physiology, Male Reproductive System
Physiology, Nasal
Physiology, Obesity Neurohormonal Appetite And Satiety Control
Physiology, Parathyroid
Physiology, Peristalsis
Physiology, Proteins
Physiology, Puberty
Physiology, Small Bowel
Physiology, Synuclein
Physiology, Thyroid Function
Physiology, Thyroid Hormone
Physiology, Urea Cycle
Physiology, Vascular
Polycystic Kidney Disease
Polycystic Kidney Disease Of Childhood
Polycythemia Vera
Polyglandular Autoimmune Syndrome Type I
Prader-Willi Syndrome
Precocious Puberty
Preconception Counseling
Pregnancy Ultrasound Evaluation
Prenatal Genetic Screening
Prenatal Screening
Progeria (Werner Syndrome)
Protein C Deficiency
Prune Belly Syndrome
Pseudohypoparathyroidism
Pulmonary Hamartoma
Radial Dysplasia (Clubhand)
Restrictive (Infiltrative) Cardiomyopathy
Rett Syndrome
Right Aortic Arches
Rotor Syndrome
Severe Combined Immunodeficiency
Short Stature
Shwachman-Diamond Syndrome
Sickle Cell Anemia
Sickle Cell Disease
Sickle Cell Trait
Spinocerebellar Ataxia
Sports Physicals
Sudden Cardiac Death
Supravalvar Aortic Stenosis (SVAS)
Sydenham Chorea
Syndactyly
Syringomyelia
Thalassemia
Thyroxine-Binding Globulin Deficiency
Tourette Syndrome And Other Tic Disorders
Truncus Arteriosus
Tuberous Sclerosis
Turcot Syndrome
Turner Syndrome
Unconjugated Hyperbilirubinemia
Universal Precautions
Urea Cycle Disorders
Vohwinkel Syndrome
Von Hippel Lindau Syndrome
Von Willebrand Disease
Whipple Disease
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wilson Disease
Wiskott-Aldrich Syndrome
Xeroderma Pigmentosum
X-linked Agammaglobulinemia
Young Syndrome