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Autosomal Dominant Disorders

Autosomal dominant inheritance means an abnormal gene from one parent can cause disease, even though the matching gene from the other;

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Polycystic Kidney Disease

This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common;

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Polycystic Kidney Disease

This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common;

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The Porphyrin Handbook

autosomal dominant disorders with incomplete penetrance. Other chapters consider the main characteristics of congenital erythropoietic porphyria;

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Current Progress in Human Genetics

autosomal dominant inheritance, X-linked and Y-linked inheritance and autosomal recessive inheritance. Human genetics is an important field that;

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Genetics and Genomics of Neurobehavioral Disorders

review the current status of research in autosomal disorders that produce such dysfunctions, examining both microdeletion disorders (Prader-Willi;

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Cystic & Idiopathic Pulmonary Fibrosis

Cystic fibrosis (CF) is one of the most common autosomal recessive disorders in the Caucasian population with an estimated incidence of 1;

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Clinical Neurogenetics, An Issue of Neurologic Clinics

; Autism/ASD; Fragile X Tremor Ataxia Syndrome (FXTAS); Lysosomal Storage Diseases; Psychiatric Disorders; Dominant Spinocerebellar Ataxias;

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Focus on Glaucoma Research

to blindness. Glaucoma occurs in several forms: chronic open-angle (primary), acute angle-closure, congenital (inherited as an autosomal;

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Trends in Glaucoma Research

to blindness. Glaucoma occurs in several forms: chronic open-angle (primary), acute angle-closure, congenital (inherited as an autosomal;

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The Official Patient's Sourcebook On Polycystic Kidney Disease

: Autosomal dominant polycystic kidney disease, Autosomal dominant polycystic kidney disease (ADPKD), Cystic Disease of the Renal Medulla, Cysts;

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Fetal and Perinatal Skeletal Dysplasias

(autosomal dominant or recessive, or non-genetic), the Mendelian Inheritance in Man number (MIM) for further reference reading, the locus (the;

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New Developments in Down Syndrome Research

syndrome; the impact of environmental risk factors on maternal meiotic errors; genomic implications of gene dosage imbalance in autosomal trisomy;

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Molecular Mechanisms Involved in the Pathogenesis of Huntington's Disease

Huntington's disease (HD) is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea;

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Hypoparathyroidism

hypocalcemia following neck surgery, as well as autoimmune, syndromic, idiopathic, and autosomal dominant etiologies. Conventional management with;

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Human Genetics

personality. The concepts of autosomal dominant and recessive inheritance, X-linked and Y-linked inheritance are vital to this field. Pedigree chart;

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Developments in Genetic Hearing Impairment

of gene localization and identification in non-syndromal autosomal recessive hearing impairment, papers on gene localization in dominant and;

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Brain Arteriovenous Malformations and Arteriovenous Fistulas

Parkes-Weber syndrome; and autosomal dominant genetic disorders such as Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu syndrome) and;

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DNA Electrophoresis Protocols for Forensic Genetics

profiling. It includes protocols for profiling of autosomal STRs, Y-STRs, X-STRs, autosomal SNPs, INDELS, Y-SNPs, mtDNA-SNPs, and mtDNA;

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Nephrology -- Dialysis -- Transplantation

Nephrology deals with the study of the function and diseases of the kidney. Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the;

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Huntington's Disease

Huntington's disease, which is also known as Huntington's chorea, is a progressive genetic autosomal disorder of the central nervous system;

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Cardiovascular Disorders

conditions are preventable. However, cardiovascular diseases remain the dominant cause of death in the world today. This book discusses the;

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Cytokines Detection by Elisa in Male Albino Rates

The book data demonstrated here showed the following points: (1) Acarus siro was the most dominant species detected in collected flour;

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Linkage Analysis Of Myopia Phenotype In Pakistan

linkage against MYP7 locus in one of the five familes with autosomal dominant mode of inheritance. Later the LOD Score for this family;

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Huntington's Disease

be an inherited disease, but 10% of all cases of HD may be due to acquired mutations of genes. It is caused due to an autosomal dominant;

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Neutropenia, An Issue of Hematology/Oncology Clinics of North America

-colony Stimulating Factor (G-CSF) Receptor Signaling Pathways ,Neutrophil elastase (ELANE) - Genetics and Pathophysiology,Autosomal recessive;

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Disorderly Eaters

eating becomes a tool for self-assertion as a rebellion against an unacceptable dominant ethos. Disorderly Eaters reveals that creative;

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