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dysmorphology

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dys·mor·phol·o·gy (dsmôr-fl-j)
n.
The branch of clinical genetics concerned with the study of structural defects, especially congenital malformations.

dysmorphology
Neonatology The systemic study of structural defects of prenatal onset, a complex field in which single or multiple primary malformations are idiopathic or related to chromosome defects–recurrence rate of 2-5%, drugs, chemicals, toxins or radiation. See Deformation, Disruption, Malformation, Multiple malformation syndrome, Sequence.


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Chapter topics include the cell, protein synthesis, gametogenesis, the place of genetics in medicine, autosomal recessive inheritance, chromosome structural abnormalities, twin studies, immunogenetics, gene mapping, dysmorphology, southern blotting, DNA profiling, an avoidance and prevention of disease.
The investigators also failed to identify an association between thimerosal-containing Rh immunoglobulin and various autism characteristics, including clinical diagnosis, IQ, gender, dysmorphology status, head size, and regressive versus early-onset autism spectrum disorder.
The first three chapters give a broad overview of dysmorphology, assessment of an infant with congenital malformation, and guiding principles of genetic counseling.
 
 
 
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