Detalhe da pesquisa
1.
The prevalence and phenotypic range associated with biallelic PKDCC variants.
Clin Genet
; 104(1): 121-126, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36896672
2.
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
Am J Hum Genet
; 87(5): 618-30, 2010 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21055719
3.
Dysmorphic and anthropometric outcomes in 6-year-old prenatally cocaine-exposed children.
Neurotoxicol Teratol
; 28(1): 28-38, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16298510
4.
Total is more than the sum of the parts: phenotyping the heart in cardiovascular genetics clinics.
Am J Med Genet A
; 131(2): 111-4, 2004 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15487010