About the Book
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 143. Chapters: Chromosomal abnormalities, Defects of cell structure, Disorders of globin and globulin proteins, Disorders of synthesis of DNA, RNA, and proteins, Enzyme defects, Hereditary cancers, Membrane transport protein disorders, Down syndrome, Turner syndrome, Crohn's disease, Adrenoleukodystrophy, Trisomy, Breast cancer, Von Hippel-Lindau disease, XYY syndrome, Warkany syndrome 2, Hemoglobinopathy, Sickle-cell disease, Episodic ataxia, Beckwith-Wiedemann syndrome, Hypophosphatasia, Congenital disorder of glycosylation, Klinefelter's syndrome, Hereditary nonpolyposis colorectal cancer, Trinucleotide repeat disorder, Thalassemia, Williams syndrome, LEOPARD syndrome, Fructose malabsorption, 1p36 deletion syndrome, Multiple endocrine neoplasia, Aneuploidy, Diamond-Blackfan anemia, Retinoblastoma, Noonan syndrome, Alpha 1-antitrypsin deficiency, 1q21.1 deletion syndrome, Multiple endocrine neoplasia type 2b, Kidney cancer, Male breast cancer, Sickle cell trait, Familial adenomatous polyposis, Edwards syndrome, Cowden syndrome, Philadelphia chromosome, Beta-thalassemia, Patau syndrome, 22q13 deletion syndrome, Hereditary angioedema, Smith-Magenis syndrome, Xeroderma pigmentosum, 1q21.1 duplication syndrome, Cystinuria, Machado-Joseph disease, Incontinentia pigmenti, 3-M syndrome, Triple X syndrome, Pendred syndrome, 17q21.3 recurrent microdeletion syndrome, Progressive familial intrahepatic cholestasis, WAGR syndrome, Stargardt disease, Hartnup disease, Cri du chat, Pallister-Killian syndrome, Danon disease, Lysinuric protein intolerance, Adrenomyeloneuropathy, XXYY syndrome, Alpha-thalassemia, Salla disease, Glucose-galactose malabsorption, 48, XXXX, Hemoglobin Lepore syndrome, Li-Fraumeni syndrome, Kostmann syndrome, Wolf-Hirschhorn syndrome, Y chromosome microdeletion, Gardner's syndrome, Chromosome abnormality, 22q11.2 dupl...
