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This can be a 3-in-1 reference publication. It supplies an entire scientific dictionary overlaying hundreds and hundreds of phrases and expressions with regards to Down syndrome. It additionally supplies wide lists of bibliographic citations. ultimately, it offers info to clients on easy methods to replace their wisdom utilizing a variety of net assets. The booklet is designed for physicians, clinical scholars getting ready for Board examinations, clinical researchers, and sufferers who are looking to get to grips with examine devoted to Down syndrome. in the event that your time is effective, this booklet is for you. First, you won't waste time looking the net whereas lacking loads of proper details. moment, the publication additionally saves you time indexing and defining entries. ultimately, you won't waste money and time printing hundreds of thousands of web content.
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Extra resources for Down Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References
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Generate_Screen • Project Title: DEFINITION AND DEVELOPMENT OF THE PHENOTYPE IN AUTISM Principal Investigator & Institution: Rogers, Sally J. O. Box 6508, Grants and Contracts Aurora, CO 800450508 Timing: Fiscal Year 2001; Project Start 01-JUN-1997; Project End 31-MAY-2002 30 Down Syndrome Summary: The overall goal of this Program Project is to define more clearly what is both familial and specific in the autism phenotype at three levels of analysis "brain, neuropsychology, and behavior" through a series of converging tests.
In collaboration with Jeanette Holden, we will also test the hypothesis that lowered maternal serum dopamine betahydroxylase (DBH), secondary to allelic differences at the DBH locus, provides a uterine environment which is part of the etiology of autism and autistic features in both idiopathic autism and Fragile X syndrome (FXS). GRNT P01HD354680001 Autism is a devastating developmental disorder with an incidence of approximately 1 in 1,000 live birth. While strongly genetically determined, specific abnormalities remain to be determined, and the clinical picture is sufficiently diffuse to implicate pathology in multiple neural systems.
These cell lines will be tested for homo/heterophilic cell adhesion using a standard cell adhesion assay. Briefly, cells will be incubated in suspension either with cells expressing the same Dscam receptor or a different one. The cells will be differentially labeled with lipophilic dyes and checked for aggregation using confocal microscopy. Dscam receptors may also interact in cis (on the same cell surface). This will be tested through transient transfection of one receptor into a stable line expressing another.