Detalhe da pesquisa
1.
Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.
Am J Med Genet
; 84(3): 184-90, 1999 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-10331587
2.
Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
Am J Med Genet
; 84(3): 217-20, 1999 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-10331595
3.
FMR1 repeat analysis in patients with ovarian dysfunction or failure.
Am J Med Genet
; 83(4): 329-30, 1999 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-10208173
4.
Frequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada.
Am J Med Genet
; 84(3): 195-7, 1999 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-10331589
5.
A novel arginine vasopressin-neurophysin II mutation causes autosomal dominant neurohypophyseal diabetes insipidus and morphologic pituitary changes.
Horm Res
; 53(5): 239-45, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-11150885