ライフサイエンスコーパス: genetic counselling

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1 he precise diagnosis and provide appropriate genetic counselling.

2 ated in other cohorts--could be relevant for genetic counselling.

3 ning for causes of sudden cardiac death, and genetic counselling.

4 , with consequent important implications for genetic counselling.

5 accurate diagnosis and providing appropriate genetic counselling.

6 us to raise issues about genetic testing and genetic counselling.

7 he provision of more accurate prognostic and genetic counselling.

8 etrance will provide crucial information for genetic counselling.

9 s still unknown in many patients, precluding genetic counselling and better understanding of the phys

10 Genetic counselling and clinical risk stratification are

11 This has important implications for genetic counselling and diagnostic service provision.

12 ffer significant prospects for more accurate genetic counselling and effective future therapies.

13 Focused genetic counselling and health education might lead to a

14 aediatric macular disease and allowed better genetic counselling and information about prognosis to b

15 an accurate diagnosis is important as it has genetic counselling and often treatment implications.

16 blish an accurate diagnosis and for reliable genetic counselling and prenatal diagnosis.

17 Our finding will aid genetic counselling and prenatal diagnosis.

18 ial genome calls for a different approach to genetic counselling and risk analysis.

19 CYLD mutations is challenging and we discuss genetic counselling and surgical interventions.

20 s provide a rational basis on which to guide genetic counselling and to tailor clinical surveillance.

21 During this time, precise diagnosis, genetic counselling, and medical management have improve

22 s this will affect the genetic causation and genetic counselling, and provide prognostic information

23 ld clinical complications, its diagnosis and genetic counselling are important to prevent inheritance

24 opriate investigations, timely treatment and genetic counselling are paramount to ameliorate the shor

25 ay be appropriate to offer Y-DNA testing and genetic counselling before starting assisted reproductiv

26 Our results could be useful in genetic counselling for carriers of this mutation and in

27 an with a son with Batten's disease came for genetic counselling for her current pregnancy.

28 from being clinically useful or relevant to genetic counselling for specific disorders, their detect

29 ychological effect of risk communication and genetic counselling has been elucidated and women's risk

30 on of patient management, and evokes broader genetic counselling implications for affected families.

31 Accurate genetic counselling in MC should be based not only upon

32 The focus of clinical genetics, and thus genetic counselling, is forecast to expand from the diag

33 nd molecular investigation and should inform genetic counselling of at-risk individuals, with the ide

34 ul in the clinical identification of IIN and genetic counselling of nystagmus patients.

35 be considered in the diagnostic work-up and genetic counselling of patients with calpainopathy and s

36 tion will be important in the management and genetic counselling of patients with Parkinson's disease

37 n should be considered in the management and genetic counselling of patients with these fatal neurode

38 g for the 185delAG mutation may be useful in genetic counselling of these women where options for det

39 They were offered genetic counselling, parental and (if appropriate) CF ca

40 Here, we predict how genetic counselling, specifically for more common diseas

41 as an autosomal recessive trait, a change in genetic counselling, testing, and surveillance is needed

42 gauge the need for appropriate diagnoses and genetic counselling to reduce the number of neonates aff

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