Detalhe da pesquisa
1.
Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Cytogenet Genome Res
; 132(4): 233-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21063078
2.
Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases.
Pharmacogenomics J
; 11(4): 287-91, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20514079
3.
Wide clinical spectrum in Zimmermann-Laband syndrome.
Genet Couns
; 22(1): 1-10, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21614982
4.
Zimmermann-Laband syndrome: further clinical delineation.
Genet Couns
; 16(3): 283-90, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16261693
5.
FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
Am J Med Genet
; 103(4): 289-94, 2001 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11746008
6.
A variant example of familial Floating-Harbor syndrome?
Genet Couns
; 14(1): 31-7, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12725587
7.
Floating-Harbor syndrome. A neuropsychological approach.
Genet Couns
; 7(4): 283-8, 1996.
Artigo
em Inglês
| MEDLINE | ID: mdl-8985732
8.
Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome.
Clin Dysmorphol
; 11(4): 243-7, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12401988
9.
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.
Br J Dermatol
; 153(6): 1216-9, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16307662
10.
Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia.
Blood Cells Mol Dis
; 35(1): 66-9, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15905108
11.
inv(9)(p24q13) in three sterile brothers.
Ann Genet
; 43(1): 51-4, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10818222
12.
Reproductive history in mothers of children with neural tube defects.
Gynecol Obstet Invest
; 49(4): 255-60, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10828709
13.
Alphoidless centromere of a familial unstable inverted Y chromosome.
Ann Genet
; 39(4): 236-9, 1996.
Artigo
em Inglês
| MEDLINE | ID: mdl-9037351
14.
The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations.
Ann Genet
; 43(2): 89-92, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10998450
15.
Madelung's deformity from a rheumatologist's point of view.
Br J Rheumatol
; 36(8): 925-6, 1997 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-9291869