Detalhe da pesquisa
1.
Prenatal diagnosis and clinical findings in a case of hexasomy 12p.
Am J Med Genet
; 47(8): 1171-4, 1993 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-8291550
2.
Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence.
Genet Med
; 1(1): 29-33, 1998.
Artigo
Inglês
| MEDLINE | ID: mdl-11261426
3.
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
Hum Genet
; 99(1): 11-7, 1997 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-9003485