Detalhe da pesquisa
1.
Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene.
Neurogenetics
; 16(1): 23-6, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25338135
2.
International trade and the neoliberal diet in Central America and the Dominican Republic: Bringing social inequality to the center of analysis.
Soc Sci Med
; 239: 112516, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31513933
3.
Non-confined long-standing blood chimerism in a spontaneous monochorionic dizygotic twin pregnancy.
Int J Gynaecol Obstet
; 148(3): 399-400, 2020 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31671208
4.
A human laterality disorder associated with a homozygous WDR16 deletion.
Eur J Hum Genet
; 23(9): 1262-5, 2015 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-25469542
5.
Cytokine secretion and NK cell activity in human ADAM17 deficiency.
Oncotarget
; 6(42): 44151-60, 2015 Dec 29.
Artigo
Inglês
| MEDLINE | ID: mdl-26683521
6.
Monozygotic multiple gestation after intracytoplasmic sperm injection and preimplantation genetic diagnosis.
Fertil Steril
; 92(6): 2037.e11-7, 2009 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-19819442
7.
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature.
Eur J Med Genet
; 52(2-3): 140-4, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19328248
8.
A patient with Prader-Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy.
Am J Med Genet A
; 129A(2): 176-9, 2004 Aug 30.
Artigo
Inglês
| MEDLINE | ID: mdl-15316980