NP-Genetics 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
Acrokeratosis Verruciformis of Hopf
Acute Ankle Sprain
Acute Intermittent Porphyria
Aggression In Hypothalamic Hamartoma
Alagille Syndrome
Albinism
Alcohol Sanitizer
Allopurinol
Alpers-Huttenlochen Syndrome (AHS, Alper Disease)
Alpha 1 Antitrypsin Deficiency
Alpha Fetoprotein (AFP, Maternal Serum Alpha Fetoprotein, MSAFP)
Alport Syndrome
Alzheimer Disease
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, Tooth Eruption
Anatomy, Thorax, Heart Anomalous Left Coronary Artery
Androgen Insensitivity Syndrome
Anemia, Iron Deficiency
Aniridia
Apert Syndrome
Arginase Deficiency (Argininemia)
Arrhythmogenic Right Ventricular Cardiomyopathy
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atlantoaxial Instability
Axenfeld Anomaly
Bartter Syndrome
Beevor Sign
Biochemistry, Chylomicron
Biochemistry, DNA Replication
Biochemistry, DNA Structure
Biochemistry, Hemoglobin Synthesis
Biochemistry, HLA Antigens
Biochemistry, LDL Cholesterol
Biochemistry, Lipids
Biochemistry, Lipoprotein Lipase
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Biochemistry, Replication and Transcription
Biochemistry, Tetrahydrofolate
Birt Hogg Dube Syndrome
Blepharitis
Blood Pressure Measurement
Brachial Plexitis (Parsonage Turner Syndrome, Brachial Neuropathy, Brachial Radiculitis)
BRCA 1 and 2
Bruton Agammaglobulinemia
C 17 Hydroxylase Deficiency
C1 Esterase Inhibitor Deficiency
Canavan Disease
Cancer, Basal Cell
Cancer, Breast
Cancer, Burkitt Lymphoma
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Colon
Cancer, Endometrial
Cancer, Hodgkin Lymphoma
Cancer, Neuroblastoma
Cancer, Renal Cell
Cancer, Retinoblastoma
Cancer, Tumor-Suppressor Genes
Cardiac Fibroma
Carney Complex
Celiac Disease
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Chediak Higashi Syndrome
Cherry Red Spot
Chest Trauma
Child Syndrome
Chorea
Chromosome Instability Syndromes
Chronic Diarrhea
Chronic Granulomatous Disease
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Lip
Coarctation of the Aorta
Cockayne Syndrome
Colitis, Ulcerative
Color Vision
Congenital Adrenal Hyperplasia
Cowden Disease (Multiple Hamartoma Syndrome)
Craniosynostosis
Creatine Phosphokinase
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crohn Disease
Crouzon Syndrome
Cutaneous Angiofibroma
Cystic Fibrosis
Cystic Fibrosis Related Diabetes (CFRD)
Danon Disease
Delayed Puberty
Diabetes, Maturity Onset in the Young (MODY)
Diamond Blackfan Anemia
DiGeorge Syndrome
Down Syndrome (Trisomy 21)
Drug Induced Gingival Overgrowth (DIGO)
Dubin Johnson Syndrome
Duchenne Muscular Dystrophy
Dystonia
Ehlers Danlos Syndrome
Electrical Alternans
Embryology, Anencephaly
Embryology, Branchial Arches
Embryology, Ectoderm
Embryology, Esophagus
Embryology, Mullerian-inhibiting Factor
Embryology, Optic Cup
EMS, Chest Injury
Epidermal Inclusion Cyst
Eptifibatide
Fabry Disease
Familial Adenomatous Polyposis
Familial Hyperlipidemia Type 2a
Familial Hypocalciuric Hypercalcemia (FHH)
Fanconi Syndrome
Fetal Alcohol Syndrome
Fibrous Dysplasia
Fragile X Syndrome
Fuchs Endothelial Dystrophy (FED)
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gardner Syndrome
Gastroesophageal Reflux Disease
Gaucher Disease
Genetics, Autosomal Recessive
Genetics, DNA Packaging
Genetics, Epigenetic Mechanism
Genetics, Gonadal Dysgenesis
Genetics, Histone Code
Genetics, Human Major Histocompatibility Complex (MHC)
Genetics, Meiosis
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
Gorlin Syndrome (Basal Cell Nevus)
Gout (Podagra)
Gynecomastia
Hand Washing (Hand Hygiene)
Health Insurance Portability and Accountability Act (HIPAA)
Health Screening
Hemiplegic Migraine
Hemochromatosis
Hemophilia A
Hepatic (Hepatocellular) Adenoma
Hepatitis A
Hereditary Angioedema
Hereditary Spherocytosis
Hirsutism
Histology, Cell Death
Histology, Male Urethra
Holt Oram Syndrome
Hurler Syndrome
Hyperbaric, Sensorineural Hearing Loss
Hypertonic Fluids
Hypertrophic Cardiomyopathy
Hypomelanosis of Ito
Hypoparathyroidism
Hypophosphatemia
Ichthyosis X-Linked
IgA Nephropathy
Impaired Bilirubin Conjugation
Imperforate Anus
Inappropriate Medical Abbreviations
Inborn Errors Of Metabolism
Influenza Vaccine
Informed Consent
Ingrown Toenails
Insulinoma
Intellectual Disability
Interleukin
Jervell and Lange Nielsen Syndrome
Job Syndrome (Hyperimmunoglobulin E)
Kallmann Syndrome
Kidney Trauma
Klinefelter Syndrome
Klippel Feil Syndrome
Lafora Disease
Language Barrier
Latex Allergy
Leber Optic Atrophy
Li Fraumeni Syndrome
Lipoma
Lynch Syndrome
Mallory Bodies
Marfan Syndrome
McCune Albright Syndrome
Medical Error Prevention
Microcytic Hypochromic Anemia
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
Neuroanatomy, Lower Motor Neuron Lesion
Neuroanatomy, Neurons
Neurocutaneous Syndromes
Neurofibromatosis
Neurofibromatosis Type 1 (Von Recklinghausen)
Neurofibromatosis Type 2
Nevus Comedonicus
Noonan Syndrome
Nursing Ethical Considerations
Nursing Grief and Loss
Open Angle Glaucoma
Ornithine Transcarbamylase Deficiency
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteochondroma
Osteogenesis Imperfecta
Patau Syndrome
Patient Confidentiality
Pediatric Functional Constipation
Pediatric Hearing Loss
Pemphigus Vegetans
Pendred Syndrome
Penicillin Allergy
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Phenylketonuria
Physiology, Airway Resistance
Physiology, Antibody
Physiology, Bile
Physiology, Cardiovascular Murmurs
Physiology, Exocrine Gland
Physiology, Factor V
Physiology, Factor XIII
Physiology, Follicle Stimulating Hormone
Physiology, Heart Sounds
Physiology, Lung Capacity
Physiology, Osmoregulation and Excretion
Physiology, Puberty
Physiology, Urea Cycle
Physiology, Vascular
Piebaldism
Poland Syndrome
Polycystic Kidney Disease
Polycystic Kidney Disease Of Childhood
Polyglandular Autoimmune Syndrome, Type II (Carpenters, Schmidt)
Precocious Puberty
Pregnancy Medications
Prenatal Screening
Primary Hyperparathyroidism
Progeria (Werner Syndrome)
Prothrombin Time
Prune Belly Syndrome
Raccoon Sign
Recognizing Alcohol and Drug Impairment in the Workplace in Florida
Research Study
Restrictive (Infiltrative) Cardiomyopathy
Rett Syndrome
Rhythm, QT Prolongation
Right Aortic Arche
Seborrheic Keratosis
Seizure, Postictal State
Severe Combined Immunodeficiency
Shwachman-Diamond Syndrome
Sickle Cell Anemia
Sickle Cell Disease
Sickle Cell Trait
Sideroblastic Anemia
Splenic Trauma
Stevens Johnson Syndrome (Toxic Epidermal Necrolysis)
Succinylcholine Chloride
Sweat Testing
Sydenham Chorea
Syndromic Sensorineural Hearing Loss (SSHL)
Syringomyelia
Thalassemia
Thyroxine-Binding Globulin Deficiency
Tort
Tourette Syndrome And Other Tic Disorders
Tracheal Bronchus
Treadmill Stress Testing
Truncus Arteriosus
Tuberous Sclerosis
Turcot Syndrome
Unconscious Patient
Urea Cycle Disorders
Von Hippel Lindau Syndrome
Von Willebrand Disease
Western Blot (Protein Immunoblot)
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wilson Disease
Wiskott-Aldrich Syndrome
Wyburn-Mason Syndrome
X-linked Agammaglobulinemia
Young Syndrome