Titlebook: Cardiovascular Genetics and Genomics; Principles and Clini Dhavendra Kumar,Perry Elliott Book 2018 Springer International Publishing AG 201

Armory

气候

https://doi.org/10.1007/978-3-319-66114-8Adult congenital heart disease; Cardiac Genomics; Familial cardiomyopathies; Gene sequencing; Inherited

植物茂盛

978-3-319-88179-9Springer International Publishing AG 2018

讲个故事逗他

25-1 - 25-95: C7Cl2F4N2 - C7H5ClF3N,fect the individual at any stage from fetal to adult life. It also encompasses abnormalities encountered in postnatal adaptation, such as persistence of the ductus arteriosus. Cardiovascular abnormalities, as a group, are the most common cause of congenital anomaly and account for around 1% of live births.

jealousy

舔食

争议的苹果

24-96 - 24-222: C6H8ClN3 - C7ClF5O, therapy, this heterogeneity remains challenging to classify and, ultimately, a combined approach is necessary. As genomic medicine progresses and we enter an era of personalised medicine, our ability to develop an organic classification system able to deal with complexity will be key.

–scent

24-1 - 24-95: C6H5Cl4N - C6H8ClNO2, help identify other individuals at risk of developing the disease phenotype. The following chapter provides insight into the genetic aetiology underlying these diverse disease processes and the clinical management of these inherited cardiomyopathies.

平项山

23-116 - 23-221: C6H4Cl2N2O2S - C6H5Cl3Sn, clinical history and pathology investigations. Genetic tests in probands and cascade family screening in clinically phenotyped families provide the basis for segregation studies that are major contributors to the assignment of a causative role of mutations in families.

思想流动

26-163 - 26-222: C8H4Cl2N2 - C8H6Cl2O,ugh it is often associated with other congenital cardiac anomalies it can also be seen in association with dilated, hypertrophic and restrictive cardiomyopathies and in the absence of any cardiac defects.