Detalhe da pesquisa
1.
Mind the Quality Gap When Banking on Dry Blood Spots.
Biopreserv Biobank
; 19(2): 136-142, 2021 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-33567235
2.
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.
Genes Immun
; 11(8): 609-21, 2010 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-20861866
3.
Complement factor H polymorphisms, renal phenotypes and age-related macular degeneration: the Blue Mountains Eye Study.
Genes Immun
; 9(3): 231-9, 2008 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-18340363
4.
Parental age in Indian patients with sporadic hereditary retinoblastoma.
Ophthalmic Epidemiol
; 7(4): 285-91, 2000 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-11262675
5.
Nongonadal neoplasia in patients with Turner syndrome.
J Environ Pathol Toxicol Oncol
; 18(4): 339-47, 1999.
Artigo
Inglês
| MEDLINE | ID: mdl-15281247
6.
Genetics of otosclerosis.
J Laryngol Otol
; 111(2): 109-12, 1997 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-9102432
7.
A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21.
J Med Genet
; 41(11): 872-6, 2004 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-15520414
8.
Effects of inbreeding on reproductive losses in Kota tribe.
Acta Genet Med Gemellol (Roma)
; 46(2): 123-8, 1997.
Artigo
Inglês
| MEDLINE | ID: mdl-9492894
9.
Human molecular cytogenetics: diagnosis, prognosis, and disease management.
Teratog Carcinog Mutagen
; Suppl 1: 225-33, 2003.
Artigo
Inglês
| MEDLINE | ID: mdl-12616613
10.
Absence of pericentromeric heterochromatin (9qh-) in a patient with bilateral retinoblastoma.
Acta Genet Med Gemellol (Roma)
; 46(4): 193-8, 1997.
Artigo
Inglês
| MEDLINE | ID: mdl-9862007
11.
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.
Hum Mol Genet
; 10(22): 2501-8, 2001 Oct 15.
Artigo
Inglês
| MEDLINE | ID: mdl-11709537