The Gale Encyclopedia of Genetic Disorders 3rd Edition by Laurie Fundukian 1414476035 978-1414476032

Volume 1: A-L; 22q13 Deletion Syndrome; Aarskog Syndrome; Aase Syndrome; Abetalipoproteinemia; Absence Of Vas Deferens; Acardia; Accutane Embryopathy; Aceruloplasminemia; Achondrogenesis; Achondroplasia; ACHOO Syndrome; Acrocallosal Syndrome; Acromegaly; Adams-Oliver Syndrome; Adelaide-Type Craniosynostosis; Adenylosuccinate Lyase Deficiency; Adrenoleukodystrophy; Aicardi Syndrome; ALA Dehydratase Deficiency. Alagille SyndromeAlbinism; Alcoholism; Alexander Disease; Alkaptonuria; Alpha-1 Antitrypsin; Alpha-Thalassemia X-Linked Mental Retardation Syndrome; Alstrom Syndrome; Alzheimer’s Disease; Amelia; Amelogenesis Imperfecta; Amniocentesis; Amyoplasia; Amyotrophic Lateral Sclerosis; Androgen Insensitivity Syndrome; Anemia, Sideroblastic X-Linked; Anencephaly; Angelman Syndrome; Ankylosing Spondylitis; Apert Syndrome; Arginase Deficiency; Arnold-Chiari Malformation; Arthrogryposis Multiplex Congenita; Arthropathy-Camptodactyly Syndrome; Asperger Syndrome; Asplenia; Asthma; Astrocytoma. Ataxia-TelangiectasiaAttention Deficit Hyperactivity Disorder; Autism; Azorean Disease;

 

Bardet-Biedl Syndrome; Barth Syndrome; Bassen-Kornzweig Syndrome; Batten Disease; Beals Syndrome; Beare-Stevenson Cutis Gyrata Syndrome; Beckwith-Wiedemann Syndrome; Beta Thalassemia; Bicuspid Aortic Valve; Biotinidase Deficiency; Bipolar Disorder; Birt-Hogg-Dube Syndrome; Bloom Syndrome; Blue Rubber Bleb Nevus Syndrome; Brachydactyly; Branchiootorenal Syndrome; Breast Cancer; Bruton Agammaglobulinemia; Burger-Grutz Syndrome;

 

Campomelic Dysplasia; Canavan Disease; Cancer; Cancer Genetics. Cardiofaciocutaneous SyndromeCarnitine Palmitoyltransferase Deficiency; Carpenter Syndrome; Caudal Dysplasia; Cayler Cardiofacial Syndrome; Celiac Disease; Central Core Disease; Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy; Cerebral Palsy; Channelopathies; Charcot-Marie-Tooth Disease; Charge Syndrome; Chediak-Higashi Syndrome; Chondrodysplasia Punctata; Chondrosarcoma; Choroideremia; Chromosomal Abnormalities; Chromosome; Cleft Lip And Palate; Chromosome Map; Cleidocranial Dysplasia; Clubfoot; Cockayne Syndrome; Coffin-Lowry Syndrome. Coffin-Siris SyndromeCohen Syndrome; Collagenopathy, Types II And XI; Coloboma; Color Blindness; Compression Neuropathy; Cone-Rod Dystrophy; Congenital Adrenal Hyperplasia; Congenital Heart Disease; Congenital Hypothyroid Syndrome; Congenital Methemoglobinemia; Conjoined Twins; Conotruncal Anomaly Face Syndrome; Corneal Dystrophy; Cornelia De Lange Syndrome; Corpus Callosum, Agenesis; Costello Syndrome; Cowden Syndrome; Crane-Heise Syndrome; Craniosynostosis; Cri Du Chat Syndrome; Crouzon Syndrome; Crouzonodermoskeletal Syndrome; Cystic Fibrosis; Cystinosis; Cystinuria