Detalhe da pesquisa
1.
Refining the activities of genetic assistants: Development of task statements applicable across practice settings.
Am J Med Genet A
; 194(4): e63487, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38041235
2.
"Learning with each other, about each other": Interdisciplinary learning among genetic counseling students and clinical health psychology residents.
J Genet Couns
; 33(1): 238-243, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37965972
3.
Insights into genetic assistant practice and the workforce in North America.
J Genet Couns
; 2023 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37106568
4.
Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk-reducing surgical decision-making practices: A mixed-methods study.
J Genet Couns
; 32(3): 728-743, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36808790
5.
Integrating genetic assistants into the workforce: An 18-year productivity analysis and development of a staff mix planning tool.
J Genet Couns
; 31(5): 1183-1192, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35598107
6.
Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38.
Pediatr Blood Cancer
; 67(10): e28623, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32790119
7.
A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families.
Am J Med Genet A
; 179(2): 206-218, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30556349
8.
Reflex Seizures in a Patient with CDKL5 Deficiency Disorder.
Can J Neurol Sci
; 46(4): 482-485, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31030687
9.
Genetic counseling in a busy pediatric metabolic practice.
J Genet Couns
; 20(1): 20-2, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20839038
10.
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants.
Eur J Hum Genet
; 29(9): 1405-1417, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33603160
11.
Chromosome microarray and undiagnosed seizures in a pediatric patient.
Can J Neurol Sci
; 41(2): 281-3, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24534047
12.
Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia.
Case Rep Pediatr
; 2012: 303096, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22928142