Results 261 to 270 of about 2,075,021 (307)
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Genetic Evaluation of Familial Cardiomyopathy

Journal of Cardiovascular Translational Research, 2008
Hereditary forms of hypertrophic, dilated, restrictive, and right ventricular cardiomyopathies are frequently seen. Patterns of inheritance include autosomal dominant, autosomal recessive, X-linked, and matrilinear. Recognition of the mode of inheritance facilitates proper clinical screening of family members in subsequent generations.
Daniel P, Judge, Nicole M, Johnson
openaire   +2 more sources

Beef Genetic Evaluations

Veterinary Clinics of North America: Food Animal Practice
Genetic evaluations in beef cattle have evolved over the past 50 years relative to the hardware or software used, the statistical methodology underpinning them, and the traits evaluated. However, the underlying premise has remained the same; to generate predictions of genetic merit such that selection decisions can be made that materialize as ...
Matthew L, Spangler, Donagh P, Berry
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Genetic evaluation of short stature

Best Practice & Research Clinical Endocrinology & Metabolism, 2011
After a proper medical history, growth analysis and physical examination of a short child, followed by radiological and laboratory screening, the clinician may decide to perform genetic testing. We propose several clinical algorithms that can be used to establish the diagnosis.
Wit, J.M., Kiess, W., Mullis, P.
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Genetic Evaluation of Dilated Cardiomyopathy

Current Cardiology Reports, 2013
Recent advances have expanded our ability to conduct a comprehensive genetic evaluation for dilated cardiomyopathy (DCM). By evaluating recent literature, this review aims to bring the reader up-to-date on the genetic evaluation of DCM. Updated guidelines have been published. Mutations in BAG3, including a large deletion, were identified in 2 % of DCM.
Ana, Morales, Ray E, Hershberger
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Parents' evaluations of genetic counselling

Patient Counselling and Health Education, 1980
Genetic counseling represents a new and important health service, but little is known about how the clients of genetic clinics actually experience and view the genetic counseling process. This paper reports on the evaluations made by clients of a genetics clinic and their recommendations for ways to improve and expand this service.
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The genetic evaluation of plant genetic resources

Genome, 1989
The characterization of the nature and extent of the genetic diversity preserved in plant genetic resources collections has received much less attention than other aspects of the discipline such as collecting and storage techniques. The workshop was designed to focus on three aspects of genetic evaluation: what is the utility and significance of ...
Brad Fraleigh, B. L. Harvey
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Genetic Evaluation of Intellectual Disabilities

Seminars in Pediatric Neurology, 2008
All children with an intellectual disability (mental retardation) or global developmental delay should have a comprehensive evaluation to establish the etiology of the disability. A specific etiologic diagnosis offers the opportunity to discuss treatment, prognosis, and genetic recurrence risk.
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Genetic Evaluation of Polyposis

Current Colorectal Cancer Reports, 2010
There is substantial ongoing work in elucidating the genetics of colorectal cancer (CRC). In this article, the state of the art and clinical application of CRC genetics for syndromic, familial, and sporadic carcinoma are discussed in detail. Clinical manifestations, genetics, diagnosis, and surveillance are discussed for major colorectal cancer ...
Angus D. Thomson   +2 more
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Genetic Evaluation for Craniofacial Conditions

Facial Plastic Surgery Clinics of North America, 2016
There are thousands of craniofacial disorders, each with a different etiology. All cases of orofacial clefts have an underlying genetic cause, ranging from multifactorial with an underlying genetic predisposition to chromosomal and single-gene etiologies.
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Genetic evaluation of the floppy infant

Seminars in Fetal and Neonatal Medicine, 2011
Hypotonia in infants in the first year of life is a common diagnostic and management challenge for pediatricians and neonatologists. Several published clinical studies have shown that a substantial proportion of cases are accounted for by genetic disorders.
A N, Prasad, C, Prasad
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