Detalhe da pesquisa
1.
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.
Am J Hum Genet
; 110(3): 499-515, 2023 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36724785
2.
A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.
Ann Neurol
; 80(4)2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27543892
3.
Why is everyone so anxious?: an exploration of stress and anxiety in genetic counseling graduate students.
J Genet Couns
; 20(3): 270-86, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21264500
4.
Adrenocortical carcinoma is a lynch syndrome-associated cancer.
J Clin Oncol
; 31(24): 3012-8, 2013 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23752102
5.
Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network.
J Clin Oncol
; 31(2): 210-6, 2013 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23233716