Detalhe da pesquisa
1.
Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
Eur J Hum Genet
; 14(7): 831-7, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16617304
2.
Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited.
Eur J Hum Genet
; 13(2): 154-60, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15508017
3.
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders.
Psychiatr Genet
; 14(3): 131-7, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15318025
4.
Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man.
Hum Genet
; 119(4): 444-50, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16493556
5.
A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities.
Am J Med Genet A
; 126A(1): 46-60, 2004 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15039973
6.
Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines.
Am J Hum Genet
; 72(3): 535-8, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12548501