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1.
Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 256-260, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-326952
2.
Identification of the origin of marker chromosome by comparative genomic hybridization / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 264-267, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813896
3.
Biological characteristics and safety evaluation of endothelial progenitor cells from the umbilical cord blood / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 466-472, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813859
4.
Mapping of pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 302-306, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-229984
5.
Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 241-245, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813900
6.
Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 246-251, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813899
7.
Expression of single chain fragment variable P1D3 antibody against shrimp white spot syndrome virus in Pichia pastoris / 生物工程学报
Chinese Journal of Biotechnology
; (12): 973-978, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-325440
8.
Fetal Membrane Derived Adherent Cells: a Novel Source for Mesenchymal Stem Cells / 中国生物工程杂志
China Biotechnology
; (12)2006.
Artículo
en Zh
| WPRIM | ID: wpr-685055
9.
A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 147-150, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-263832
10.
Hotspot of the mutations of keratin 9 gene in a diffuse palmoplantar keratoderma family / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 521-524, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-813515
11.
Confirmation of the extra small chromosome in abnormality karyotype by PCR and FISH / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 657-659, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-813455
12.
Molecular analysis of SLC26A4 gene in a Chinese deafness family / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 376-379, 2005.
Artículo
en Inglés
| WPRIM | ID: wpr-280047
13.
A minidystrophin-EGFP fusion gene expressed in Cos-7 cells mediated by human source vector / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 493-496, 2005.
Artículo
en Inglés
| WPRIM | ID: wpr-280017
14.
Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3) / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 392-394, 2004.
Artículo
en Zh
| WPRIM | ID: wpr-328868
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