Detalhe da pesquisa
1.
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia.
J Med Genet
; 43(2): 187-92, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15908568
2.
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.
Am J Med Genet
; 43(3): 554-60, 1992 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-1605248
3.
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation.
Am J Med Genet
; 100(1): 85-6, 2001 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11337756
4.
Localization of human elav-like neuronal protein 1 (Hel-N1) on chromosome 9p21 by chromosome microdissection polymerase chain reaction and fluorescence in situ hybridization.
Genomics
; 36(1): 189-91, 1996 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-8812435
5.
Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique.
Genomics
; 53(3): 296-9, 1998 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-9799595
6.
Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.
Cytogenet Cell Genet
; 68(1-2): 67-70, 1995.
Artigo
em Inglês
| MEDLINE | ID: mdl-7956363
7.
Assignment of a human voltage-dependent sodium channel alpha-subunit gene (SCN6A) to 2q21-q23.
Genomics
; 19(2): 395-7, 1994 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-8188276