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1 etrance will provide crucial information for 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 e mutations is an important part of pre-test genetic counselling.
5 , with consequent important implications for genetic counselling.
6 accurate diagnosis and providing appropriate genetic counselling.
7 us to raise issues about genetic testing and genetic counselling.
8 he provision of more accurate prognostic and genetic counselling.
9 diagnosis is needed for a timely therapy and genetic counselling.
10 edicting prognosis and providing appropriate genetic counselling.
11 ity of pathogenicity assessment for accurate genetic counselling.
12 ng a major transformation in the practice of genetic counselling.
13 ce pattern and consequently the clinical and genetic counselling.
14 fs between laboratories pose a challenge for genetic counselling.
15 AB32 Ser71Arg needs to be assessed to inform genetic counselling.
16 he precise diagnosis and provide appropriate genetic counselling.
17 AD study allow for data-driven, differential genetic counselling across the spectrum of different AAO
18 s still unknown in many patients, precluding genetic counselling and better understanding of the phys
19 d risk of subsequent malignant neoplasms via genetic counselling and clinical genetic testing for can
20                                              Genetic counselling and clinical risk stratification are
21          This has important implications for genetic counselling and diagnostic service provision.
22                                              Genetic counselling and disclosure of all results was st
23 ffer significant prospects for more accurate genetic counselling and effective future therapies.
24 ficiency (with or without anaemia) and AVMs, genetic counselling and evaluation of at-risk family mem
25 and adults, as well as emergency management, genetic counselling and family planning, for patients wi
26                                      Focused genetic counselling and health education might lead to a
27 aediatric macular disease and allowed better genetic counselling and information about prognosis to b
28 an accurate diagnosis is important as it has genetic counselling and often treatment implications.
29 Ds in Iran, hopefully contributing to better genetic counselling and patient management in the respec
30 blish an accurate diagnosis and for reliable genetic counselling and prenatal diagnosis.
31                         Our finding will aid genetic counselling and prenatal diagnosis.
32 243A>G variant can help inform more tailored genetic counselling and prognostication in routine clini
33 ial genome calls for a different approach to genetic counselling and risk analysis.
34  genetic testing results, diagnostic yields, genetic counselling and selection of therapy, as well as
35 CYLD mutations is challenging and we discuss genetic counselling and surgical interventions.
36 diagnostic odysseys and facilitates accurate genetic counselling and tailored specialist management.
37                   This must be considered in genetic counselling and testing by ensuring to use compr
38 s provide a rational basis on which to guide genetic counselling and to tailor clinical surveillance.
39         During this time, precise diagnosis, genetic counselling, and medical management have improve
40 s this will affect the genetic causation and genetic counselling, and provide prognostic information
41 ld clinical complications, its diagnosis and genetic counselling are important to prevent inheritance
42 opriate investigations, timely treatment and genetic counselling are paramount to ameliorate the shor
43 ation of extraocular symptoms and meaningful genetic counselling are warranted for patients with nHON
44 ay be appropriate to offer Y-DNA testing and genetic counselling before starting assisted reproductiv
45 ed DNA-based diagnosis, potentially enabling genetic counselling, care pathways and eligibility for g
46 is uplifted genetic diagnosis should improve genetic counselling, enables family cascade screening, o
47 ogical basis, and vitally, enable meaningful genetic counselling for affected individuals and their f
48               Our results could be useful in genetic counselling for carriers of this mutation and in
49 and its useful translation into clinical and genetic counselling for families.
50 an with a son with Batten's disease came for genetic counselling for her current pregnancy.
51 der to develop collaborative strategies with genetic counselling for optimal care of patients and the
52 anagement of these patients, and help in the genetic counselling for patients and their families.
53 to graft-versus-host disease prophylaxis and genetic counselling for relatives.
54  from being clinically useful or relevant to genetic counselling for specific disorders, their detect
55 te risk by adhering to screening guidelines, genetic counselling, genetic risk testing, and other scr
56 ychological effect of risk communication and genetic counselling has been elucidated and women's risk
57 on of patient management, and evokes broader genetic counselling implications for affected families.
58 ncrease diagnostic yield and can help inform genetic counselling in families with albinism.
59  have potentially important implications for genetic counselling in HD-affected families.
60                                     Accurate genetic counselling in MC should be based not only upon
61 tation is identified in an affected patient, genetic counselling is proposed for first-degree relativ
62     The focus of clinical genetics, and thus genetic counselling, is forecast to expand from the diag
63 nd molecular investigation and should inform genetic counselling of at-risk individuals, with the ide
64           These results should enable better genetic counselling of individuals with Xp22.31 microdup
65 ul in the clinical identification of IIN and genetic counselling of nystagmus patients.
66  be considered in the diagnostic work-up and genetic counselling of patients with calpainopathy and s
67 tion will be important in the management and genetic counselling of patients with Parkinson's disease
68 n should be considered in the management and genetic counselling of patients with these fatal neurode
69 g for the 185delAG mutation may be useful in genetic counselling of these women where options for det
70                            They were offered genetic counselling, parental and (if appropriate) CF ca
71 iagnosis has helped our patients with IEI in genetic counselling, prenatal diagnosis, and accessing a
72 yotrophic Lateral Sclerosis (ALS) can inform genetic counselling, prognosis and, in the light of inco
73 is, which restricts their access to in-depth genetic counselling, reproductive options and clinical t
74                         Here, we predict how genetic counselling, specifically for more common diseas
75 ic alterations holds the potential to direct genetic counselling, testing and possibly monitoring for
76 as an autosomal recessive trait, a change in genetic counselling, testing, and surveillance is needed
77 ry pathogenic mtDNA variants require bespoke genetic counselling to determine their reproductive opti
78 gauge the need for appropriate diagnoses and genetic counselling to reduce the number of neonates aff
79  genetic testing with results disclosure and genetic counselling to those in the US (including Puerto