Detalhe da pesquisa
1.
Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints.
Am J Med Genet A
; 152A(12): 3074-83, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21108392
2.
Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays.
Hum Mutat
; 27(5): 467-73, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16619270
3.
Safety and immunogenicity of a single dose 23-valent pneumococcal polysaccharide vaccine in Russian subjects.
Hum Vaccin Immunother
; 12(8): 2142-2147, 2016 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27149114
4.
Vaccination of adults with 23-valent pneumococcal polysaccharide vaccine induces robust antibody responses against pneumococcal serotypes associated with serious clinical outcomes.
Hum Vaccin Immunother
; 12(8): 2135-2141, 2016 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27002793
5.
An open-label, randomized study of a 9-valent human papillomavirus vaccine given concomitantly with diphtheria, tetanus, pertussis and poliomyelitis vaccines to healthy adolescents 11-15 years of age.
Pediatr Infect Dis J
; 34(6): 627-34, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25831420
6.
Pregnancy and infant outcomes in the clinical trials of a human papillomavirus type 6/11/16/18 vaccine: a combined analysis of five randomized controlled trials.
Obstet Gynecol
; 114(6): 1179-1188, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19935017
7.
Symptomatic Chiari I malformation in Kabuki syndrome.
Am J Med Genet A
; 132A(3): 273-5, 2005 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-15523623
8.
Immune abnormalities are a frequent manifestation of Kabuki syndrome.
Am J Med Genet A
; 135(3): 278-81, 2005 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15887282
9.
Craniosynostosis: another feature of the 22q11.2 deletion syndrome.
Am J Med Genet A
; 136A(4): 358-62, 2005 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16001439
10.
Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome.
Am J Med Genet A
; 128A(4): 340-51, 2004 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15264279