Genetics-Medical Student Articles

Article Name

21 Hydroxylase Deficiency
5 Alpha Reductase Deficiency
A Review Of Hereditary Colorectal Cancers
Abetalipoproteinemia
Acanthocytosis
Acoustic Neuroma (Vestibular Schwannoma)
Acrodermatitis Enteropathica
Acrokeratoelastoidosis
Acute Intermittent Porphyria
Addison Disease
Afatinib
Albinism
Alpers-Huttenlochen Syndrome (AHS, Alper Disease)
Alpha 1 Antitrypsin Deficiency
Alpha 1 Antitrypsin Mutation
Alpha Fetoprotein (AFP, Maternal Serum Alpha Fetoprotein, MSAFP)
Alport Syndrome
Amyloid Beta Peptide
Anatomy, Head and Neck, Eye Iris Sphincter Muscle
Anatomy, Head and Neck, Parathyroid, Ectopic Glands
Anatomy, Head and Neck, Tooth Eruption
Androgen Insensitivity Syndrome
Aniridia
Ankylosing Spondylitis
Anosmia
Aplastic Anemia
Apoptosis
Ataxia Telangiectasia (Louis-Bar Syndrome)
Autism Spectrum Disorder (Regressive Autism, Child Disintegrative Disorder)
Biochemistry, Apolipoprotein B
Biochemistry, Chloride Channels
Biochemistry, DNA Replication
Biochemistry, DNA Structure
Biochemistry, Dopamine Receptors
Biochemistry, Hemoglobin Synthesis
Biochemistry, HLA Antigens
Biochemistry, LDL Cholesterol
Biochemistry, Lipids
Biochemistry, Lipoprotein Lipase
Biochemistry, Polymerase Chain Reaction (PCR)
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Biochemistry, Replication and Transcription
Biochemistry, Tetrahydrofolate
Birt Hogg Dube Syndrome
Bleeding Time
Bone Age
Bone Marrow Failure
BRCA 1 and 2
Bruton Agammaglobulinemia
C 17 Hydroxylase Deficiency
C1 Esterase Inhibitor Deficiency
Canavan Disease
Cancer, Basal Cell
Cancer, Burkitt Lymphoma
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Colon
Cancer, Hodgkin Lymphoma
Cancer, Lung
Cancer, Neuroblastoma
Cancer, Pancreas
Cancer, Renal Cell
Cancer, Retinoblastoma
Cancer, Tumor-Suppressor Genes
Cardiac Disease In Pregnancy
Carney Complex
Celiac Disease
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Chediak Higashi Syndrome
Cherry Red Spot
Cholinesterase Inhibitors
Chorea
Chromosome Instability Syndromes
Chronic Diarrhea
Chronic Granulomatous Disease
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Lip
Coarctation of the Aorta
Colitis, Ulcerative
Color Vision
Corneal Graft Rejection
Cowden Disease (Multiple Hamartoma Syndrome)
Creatine Phosphokinase
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crohn Disease
Crouzon Syndrome
Cystic Fibrosis
Danon Disease
Delayed Puberty
Diamond Blackfan Anemia
DiGeorge Syndrome
Down Syndrome (Trisomy 21)
Duchenne Muscular Dystrophy
Dystonia
Dystrophinopathies
Ehlers Danlos Syndrome
Embryology, Amniotic Fluid
Embryology, Central Nervous System
Embryology, Ectoderm
Embryology, Esophagus
Embryology, Mullerian-inhibiting Factor
Embryology, Optic Cup
Embryology, Week 2-3
Eptifibatide
Fabry Disease
Factor V Leiden Deficiency
Familial Adenomatous Polyposis
Familial Hyperlipidemia Type 2a
Familial Hypocalciuric Hypercalcemia (FHH)
Fanconi Syndrome
Female Development
Fetal Alcohol Syndrome
Fibrous Dysplasia
Fragile X Syndrome
Fructosamine
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gardner Syndrome
Gaucher Disease
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)
Gout (Podagra)
Gynecomastia
Health Insurance Portability and Accountability Act (HIPAA)
Health Screening
Hemiplegic Migraine
Hemochromatosis
Hemophilia A
Hepatitis A
HER2
Hereditary Angioedema
Hereditary Spherocytosis
Histology, Cell Death
Histology, Mast Cells
Histology, Parathyroid Gland
Hurler Syndrome
Hyperbaric, Sensorineural Hearing Loss
Hypertonic Fluids
Hypertrophic Cardiomyopathy
Hypophosphatemia
Ichthyosis X-Linked
Imperforate Anus
Inborn Errors Of Metabolism
Influenza Vaccine
Insulin Resistance
Intellectual Disability
Kallmann Syndrome
Klinefelter Syndrome
Lafora Disease
Li Fraumeni Syndrome
Lynch Syndrome
Mallory Bodies
Marfan Syndrome
McCune Albright Syndrome
Medical Ethics
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
Neuroanatomy, Cranial Nerve 7 (Facial)
Neuroanatomy, Neurons
Neurocutaneous Syndromes
Neurofibromatosis
Neurofibromatosis Type 1 (Von Recklinghausen)
Neurofibromatosis Type 2
Noonan Syndrome
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteogenesis Imperfecta
Paget Disease
Patau Syndrome
Pediatric Functional Constipation
Pediatric Hearing Loss
Pendred Syndrome
Peutz-Jeghers Syndrome
PHACE Syndrome
Phenylketonuria
Physiology, Antibody
Physiology, Bile
Physiology, Connective Tissue
Physiology, Follicle Stimulating Hormone
Physiology, Leukotrienes
Physiology, Puberty
Physiology, Urea Cycle
Physiology, Vascular
Polycystic Kidney Disease
Precocious Puberty
Preconception Counseling
Prenatal Screening
Progeria (Werner Syndrome)
Prune Belly Syndrome
Pseudohypoparathyroidism
Restrictive (Infiltrative) Cardiomyopathy
Rett Syndrome
Right Aortic Arche
Severe Combined Immunodeficiency
Shwachman-Diamond Syndrome
Sickle Cell Anemia
Sickle Cell Trait
Sydenham Chorea
Syringomyelia
Thalassemia
Thyroxine-Binding Globulin Deficiency
Tourette Syndrome And Other Tic Disorders
Truncus Arteriosus
Tuberous Sclerosis
Turcot Syndrome
Universal Precautions
Urea Cycle Disorders
Von Hippel Lindau Syndrome
Von Willebrand Disease
Western Blot (Protein Immunoblot)
Williams Syndrome
Wilson Disease
Wiskott-Aldrich Syndrome
X-linked Agammaglobulinemia
Young Syndrome