Detalhe da pesquisa
1.
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.
Hum Mutat
; 33(4): 728-40, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22290657
2.
Cytogenetic characterization and H-ras associated transformation of immortalized human mammary epithelial cells.
Cancer Cell Int
; 6: 15, 2006 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-16729884
3.
Activation of the chromosome 19q microRNA cluster in sporadic and androgenetic-biparental mosaicism-associated hepatic mesenchymal hamartoma.
Pediatr Dev Pathol
; 17(2): 75-84, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24555441
4.
Chronic myelogenous leukemia presenting in blast phase with nodal, bilineal myeloid sarcoma and T-lymphoblastic lymphoma in a child.
Pediatr Dev Pathol
; 16(2): 91-6, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23171293
5.
A report of dizygous monochorionic twins.
N Engl J Med
; 349(2): 154-8, 2003 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-12853588
6.
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization.
Mol Cytogenet
; 1: 7, 2008 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-18471320
7.
A case of true hermaphroditism reveals an unusual mechanism of twinning.
Hum Genet
; 121(2): 179-85, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17165045
8.
A Gender Assessment Team: experience with 250 patients over a period of 25 years.
Genet Med
; 9(6): 348-57, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17575501
9.
Extended lifespan of Barrett's esophagus epithelium transduced with the human telomerase catalytic subunit: a useful in vitro model.
Carcinogenesis
; 24(7): 1183-90, 2003 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12807723
10.
Progenitor cell involvement is predictive of response to induction chemotherapy in paediatric acute myeloid leukaemia.
Br J Haematol
; 123(3): 431-5, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14617001
11.
Primary pulmonary dysgenesis in velocardiofacial syndrome: a second patient.
Am J Med Genet A
; 121A(2): 177-9, 2003 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-12910501