THE GALE ENCYCLOPEDIA OF GENETIC DISORDERS PDF
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THE MIT PRESS THE MIT ENCYCLOPEDIA OF COMMUNICATION DISORDERS OCT 2003
Traumatic brain injury (TBI ) refers to injuries to the brain that involve rapid acceleration and deceleration, whereby the brain is whipped back and forth in a quick motion, which results in compromised neurological function (Levin, Benton, and Grossman, 1982). The goal of
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THE GALE ENCYCLOPEDIA OF NEUROLOGICAL DISORDERS VOL 2 PART 1 POT
preponderance of males with MMA; estimates of the male to female ratio range from 5:1 to 13:1.
Causes and symptoms
As of 2004, the underlying cause or causes for MMA remain unresolved. Most cases are sporadic and occur in an individual without a family history[r]
Causes and symptoms
As of 2004, the underlying cause or causes for MMA remain unresolved. Most cases are sporadic and occur in an individual without a family history[r]
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THE GALE ENCYCLOPEDIA OF NEUROLOGICAL DISORDERS VOL 1 PART 1 PPS
Description
The condition was first described in 1906 by Alois Alzheimer, a German physician. Alzheimer characterized two abnormal structures in the brain of a woman with de- mentia that are now considered the hallmarks of the dis- ease: amyloid plaques an[r]
The condition was first described in 1906 by Alois Alzheimer, a German physician. Alzheimer characterized two abnormal structures in the brain of a woman with de- mentia that are now considered the hallmarks of the dis- ease: amyloid plaques an[r]
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SLMSuite: A suite of algorithms for segmenting genomic profiles
The identification of copy number variants (CNVs) is essential to study human genetic variation and to understand the genetic basis of mendelian disorders and cancers. At present, genome-wide detection of CNVs can be achieved using microarray or second generation sequencing (SGS) data.
ADVANCES IN THE STUDY OF GENETIC DISORDERS POTX
TBX19 (1q), SOX2 (3q) and SOX3 (Xq). Mutations occurring in PROP1 are the most frequent
genetic cause of hereditary CPHD, and they are inherited as autosomal recessives. Mutations in PROP1 are associated with progressive endocrine deficiencies highly variable in bot[r]
genetic cause of hereditary CPHD, and they are inherited as autosomal recessives. Mutations in PROP1 are associated with progressive endocrine deficiencies highly variable in bot[r]
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