Detalhe da pesquisa
1.
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.
Nat Commun
; 13(1): 6463, 2022 10 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36309498
2.
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL.
Eur J Hum Genet
; 21(10): 1112-9, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23443030
3.
Congestive heart failure in renal transplant recipients: risk factors, outcomes, and relationship with ischemic heart disease.
J Am Soc Nephrol
; 13(4): 1084-1090, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11912270
4.
Electrocardiographic left ventricular hypertrophy in renal transplant recipients: prognostic value and impact of blood pressure and anemia.
J Am Soc Nephrol
; 14(2): 462-8, 2003 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-12538748