Nurse-Genetics Clinical (GCN) Articles

Article Name

Acoustic Neuroma (Vestibular Schwannoma)
Acquired Angioedema
Acrodermatitis Enteropathica
Acrokeratosis Verruciformis of Hopf
Adrenal Hypoplasia
Alagille Syndrome
Alpers-Huttenlocher Syndrome (AHS, Alper Disease)
Alpha 1 Antitrypsin Deficiency
Alpha 1 Antitrypsin Mutation
Alpha Thalassemia (Hemoglobin H Disease)
Alport Syndrome
Alzheimer Disease
Anatomy, Abdomen and Pelvis, Bowman Capsule
Anatomy, Bony Pelvis and Lower Limb, Foot
Anatomy, Head and Neck, Eye Iris Sphincter Muscle
Androgen Insensitivity Syndrome
Angioid Streaks (Knapp Streaks)
Angiokeratoma Circumscriptum
Aortic Insufficiency
Aortic Regurgitation
Arginase Deficiency (Argininemia)
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atrial Septal Defect (ASD)
Bacterial DNA Mutations
BAX Gene
Becker Muscular Dystrophy
Beckwith Wiedemann Syndrome
Bicuspid Aortic Valve
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, Glycogenolysis
Biochemistry, HLA Antigens
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
Birt Hogg Dube Syndrome
Blue Nevus
Breast Cancer
Brugada Syndrome
Cafe Au Lait Macules
Canavan Disease
Cancer, Acute Myeloid Leukemia (AML, Erythroid Leukemia, Myelodysplasia-Related Leukemia, BCR-ABL Chronic Leukemia)
Cancer, Ampullary
Cancer, Burkitt Lymphoma
Cancer, Lung Small Cell (Oat Cell)
Cancer, Neuroblastoma
Cancer, Renal
Cancer, Retinoblastoma
Carney Complex
Carnitine Deficiency
Caroli Disease
Cerebral Amyloid Angiopathy
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
CHARGE Syndrome
Chediak Higashi Syndrome
Child Syndrome
Chromosome Instability Syndromes
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Hand (Ectrodactyly, Split Hand)
Congenital Adrenal Hyperplasia
Congenital Diaphragmatic Hernia
Congenital Muscular Dystrophy
Cornelia de Lange Syndrome
Cyanotic Heart Disease
Cyclic Neutropenia
Cystic Fibrosis
Cystic Fibrosis And Liver Disease
Cystic Fibrosis Related Diabetes (CFRD)
Danon Disease
Dermal Melanocytosis (Mongolian Spot), Congenital
Diamond Blackfan Anemia
DiGeorge Syndrome
Down Syndrome (Trisomy 21)
Duchenne Muscular Dystrophy
Ehlers Danlos Syndrome
Embryology, Amniotic Fluid
Embryology, Central Nervous System
Embryology, Ectoderm
Embryology, Eye
Embryology, Eye Malformations
Embryology, Pharyngeal Pouch
Embryology, Rectum and Anal Canal
Embryology, Sexual Development
Endometrial Cancer
Eyelid Coloboma
Fabry Disease
Facioscapulohumeral Muscular Dystrophy (FSHD)
Familial Adenomatous Polyposis
Familial Hypercholesterolemia
Familial Hyperlipidemia Type 1
Familial Hyperlipidemia Type 2a
Fatal Familial Insomnia
Fragile X Syndrome
Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance)
Fuchs Endothelial Dystrophy (FED)
GABA Receptor
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, Mosaicism
Genetics, Nondisjunction
Genetics, Somatic Mutation
Genetics, Transposons
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Genetics, X-Linked Inheritance
Gitelman Syndrome
Glanzmann Thrombasthenia
Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type II (Pompe Disease)
Hartnup Disease
Hemiplegic Migraine
Hemoglobin C Disease
Hemolytic Diseases Of The Newborn
Hemophilia A
Hereditary Fructose Intolerance
Hereditary Spherocytosis
Histolology, Platelets
Holt Oram Syndrome
Huntington Disease
Hurler Syndrome
Hypertrophic Cardiomyopathy
Hypokalemic Periodic Paralysis
Hypomelanosis of Ito
Inborn Errors Of Metabolism
Insulin Resistance
Intellectual Disability
Jacobs (XYY) Syndrome
Klinefelter Syndrome
Lesch Nyhan Syndrome
Li-Fraumeni Syndrome
Lipoid Pneumonia
Lisch Nodules
Lynch Syndrome
Malabsorption Syndromes
Maple Syrup Urine Disease
Marfan Syndrome
McCune Albright Syndrome
Medullary Sponge Kidney
Multiple Endocrine Neoplasia Type 1 (MEN I, Wermer Syndrome)
Myeloproliferative Neoplasms
Myoclonic Epilepsy and Ragged Red Fibers (MERF)
Myotonic Dystrophy
Neurofibromatosis Type 1 (Von Recklinghausen)
Neurofibromatosis Type 2
Niemann-Pick Disease
Noonan Syndrome
Open Angle Glaucoma
Optic Nerve Glioma
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteogenesis Imperfecta
Pancrelipase Therapy
Patau Syndrome
Pediatric Functional Constipation
Pendred Syndrome
Pernio (Chilblains)
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Physiology, Gluconeogenesis
Physiology, Obesity Neurohormonal Appetite And Satiety Control
Physiology, Puberty
Physiology, Thyroid Function
Polycystic Kidney Disease
Polycystic Kidney Disease Of Childhood
Polyglandular Autoimmune Syndrome Type I
Prader-Willi Syndrome
Precocious Puberty
Pregnancy Ultrasound Evaluation
Prenatal Genetic Screening
Prothrombin Time
Prune Belly Syndrome
Rett Syndrome
Right Aortic Arches
Short Stature
Shwachman-Diamond Syndrome
Sickle Cell Anemia
Sickle Cell Disease
Sickle Cell Trait
Spinocerebellar Ataxia
Sports Physicals
Sturge-Weber Syndrome
Sudden Cardiac Death
Sweat Testing
Syndromic Sensorineural Hearing Loss (SSHL)
Thyroxine-Binding Globulin Deficiency
Trisomy 13
Tuberous Sclerosis
Tubular Adenoma
Turner Syndrome
Urea Cycle Disorders
Vaginal Cancer
Vascular Ring Double Aortic Arch
Von Hippel Lindau Syndrome
Whipple Disease
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wilson Disease
Wiskott-Aldrich Syndrome
Xeroderma Pigmentosum