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An Introduction to G6PD Deficiency, Oracle of Endor
Target Audience, Purpose, Introduction, Contents, Links
Facts About Fragile X Syndrome, National Institute of Child Health and Human Development
Introduction, Inheritance, Testing For Fragile X Carrier. Prenatal Testing, Diagnosing And Treating Fragile X Syndrome, Physical Characteristics, Behavioral Characteristics, Mental Impairment, Speech, Language, And Learning Disabilities, Medical Problems, Education Of Children With Fragile X, Additional Therapies, Future Research, Sources Of Information
Favism, Oralce of Endor
FAVISM: An acute hemolytic anemia, usually in persons of Mediterranean area descent, occurring when an individual with glucose-6-phosphate dehydrogenase deficiency of erythrocytes eats the beans or inhales the pollen of Vicia faba.
G6PD Deficiency,
G6PD Deficiency / About g6pd deficiency
G6PD Deficiency,
Q & A about G6PD Deficiency
Glucose-6-Phosphate Dehydrogenase Deficiency, Karoo LaunchPad
Introduction, Genetics, Biochemistry, Pharmaceutical Significance, Diagnosis & Management, Conclusion, Acknowledgement
Human Mitochondrial Genome, Emory University
MITOMAP : A Human Mitochondrial Genome Database / About human mitochondrial genome
Human Mitochondrial Genome, NCI-Frederick
Morbidity Map of the Human Mitochondrial Genome 1997 / About human mitochondrial genome
Hunter Syndrome, IowaClinic
Alternative Names, Definition, Causes, Incidence And Risk Factors
Klinefelter Syndrome, IowaClinic
Alternative Names, Definition, Causes, Incidence, And Risk Factors
Lesch-Nyhan Syndrome, IowaClinic
Definition, Causes, Incidence And Risk Factors
Leukodystrophy, United Leukodystrophy Foundation
Leukodystrophy / About leukodystrophy. Introduction, Patterns Of Inheritance, Adrenoleukodystrophy, Aicardi-Goutieres Syndrome, Alexanders Disease, CACH, CADASIL, Canavan Disease, Cerebrotendinous Xanthomatosis, Krabbe Disease, Metachromatic Leukodystrophy, Neonatal Adrenoleukodystrophy, Ovarioleukodystrophy Syndrome, Pelizaeus-Merzbacher Disease, Refsum Disease, Van der Knaap Syndrome, Zellweger Syndrome
MELAS Syndrome, Washington University in St.Louis
MELAS (Mitochondrial Encephalomyopathy; Lactic Acidosis; Stroke) / About melas syndrome. Inheritance, MtDNA Point Mutations, Clinical Syndrome, Genetic Counseling : A3423G Mutation, Laboratory
Menkes Disease, National Center for Biotechnology Information
About Menkes' Disease and ATP7A gene
Menkes Syndrome, OMIM
Description, Clinical Features, Biochemical Features, Other Features, Cytogenetics, Mapping, Molecular Genetics, Diagnosis, Clinical Management, Population Genetics, Animal Model, References, See Also, Contributors, Creation Date, Edit History, Mini-MIM, Clinical Synopsis
Mitochondria, Cognitive Enhancement Research Institute
Mitochondrial Nutrition, Aging and Cognition / About mitochondrial nutrition, aging and cognition. Mitochondrial Aging, Parkinson's Disease, Cardiolipin And ALC, Coenzyme Q, Coenzyme 1, Lipoic Acid, Supplementation, Cognitive Enhancement
Mitochondria, University of Texas Medical Branch
Mitochondria : Architecture Dictates Function / About structure of mitochondria. Substructural Organization, Powerhouse Organization, Inner Membrane Substructure, Mitochondrial Lifecycle, Mitochondrial Membrane Permeability, Import Signals
Mitochondrial Disease, CPMCnet
Mitochondrial Genetics and the Molecular Basis of Human Mitochondrial Disease / About mitochondrial disease
Mitochondrial Disorders, Washington University of St.Louis
Mitochondrial Disorders / About mitochondrial disorders. Mitochondria DNA, Nuclear Encoded Proteins, Mitochondrial Disorders
Mitochondrial Inheritance, Nontraditional Inheritance
Mitochondrial Inheritance / Nontraditional Inheritance / Vol.10 Winter,1994
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