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1 ne and will soon be a staple in research and clinical genetics.
2 olely for medical reasons, by specialists in clinical genetics.
3  limitations of use of ethical guidelines in clinical genetics.
4 d concern about the ethical issues raised by clinical genetics.
5 cation in human genomics and the practice of clinical genetics.
6 h each child having a mean of 19 tests and 4 clinical genetics and 4 nongenetics specialist consultat
7 profile will provide information relevant to clinical genetics and genetic counseling and should yiel
8 aluate gene essentiality has applications in clinical genetics and may offer insights for drug develo
9             PURPOSE OF REVIEW: The fields of clinical genetics and pharmacogenetics are rapidly expan
10 t, can subsequently be shared with the wider clinical genetics and research communities.
11                                 The focus of clinical genetics, and thus genetic counselling, is fore
12 ES) represents a significant breakthrough in clinical genetics as a powerful tool for etiological dis
13  Improved understanding of the molecular and clinical genetics associated with these lesions will lik
14 CNV/aneuploidy detection with application to clinical genetics, cancer and disease association studie
15 tients with breast cancer from familial- and clinical genetics center-based studies were 0.5%, 1.3%,
16 received counseling at 1 of 12 participating clinical genetics centers.
17 on of such variants represents a significant clinical-genetics challenge.
18 ents one of the main challenges faced by the clinical genetics community today.
19 er centers of 86 adult patients referred for clinical genetics evaluation after diagnosis of SN.
20                                              Clinical genetics evaluation is warranted for patients w
21 thogenic CNVs were noted to be dysmorphic on clinical genetics examination.
22      One of the most perplexing questions in clinical genetics is why patients with identical gene mu
23 nical impact on the diagnostic capability of clinical genetics laboratories.
24 e-exome sequencing tests were performed at a clinical genetics laboratory in the United States.
25  more frequently used based on review of the clinical genetics literature (2011-2017).
26 f this new cytogenetic test in areas outside clinical genetics may help to determine which patients w
27                            The molecular and clinical genetics of familial GEP NETs have been further
28 prospectively offered genetic counseling and clinical genetics risk assessment (group 1).
29  age younger than 50 years, evaluated by the clinical genetics service at a single tertiary care canc
30 -control study and 14 were identified from a clinical genetics service.
31  cost sharing should contribute to improving clinical genetics services and associated outcomes in th
32 bulatory outpatient clinics of the Victorian Clinical Genetics Services at the Royal Children's Hospi
33 These findings demonstrate important gaps in clinical genetics services.
34                                 In a general clinical genetics setting, the current diagnostic rate i
35 sly known 4p16.3 locus, and experimental and clinical genetics studies have shown both FGFRL1 and hsa
36 dyskeratosis congenita (DC), on the basis of clinical genetics studies, for their effects on the dysk
37 vidual research participants via their local clinical genetics team.
38   In addition, with emerging high-resolution clinical genetics testing, new polymorphisms must be ana
39 xt generation sequencing gains a foothold in clinical genetics, there is a need for annotation tools
40 ring a spectrum of approaches from human and clinical genetics to the utilization of model organism s
41 ure of reproductive biology: how advances in clinical genetics will provide special opportunities to
42  Oncologic treatment and outcomes as well as clinical genetics work-up were examined.

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