Detalles de la búsqueda
1.
Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis / 亚洲男科学杂志(英文版)
Asian Journal of Andrology
; (6): 58-65, 2023.
Artículo
en Inglés
| WPRIM | ID: wpr-971003
2.
A novel homozygous frameshift mutation in / 亚洲男科学杂志(英文版)
Asian Journal of Andrology
; (6): 197-204, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-879740
3.
Improving native human sperm freezing protection by using a modified vitrification method / 亚洲男科学杂志(英文版)
Asian Journal of Andrology
; (6): 91-96, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-879718
4.
Phenotypic and molecular characteristics of androgen insensitivity syndrome patients / 亚洲男科学杂志(英文版)
Asian Journal of Andrology
; (6): 473-478, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-1009610
5.
A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 87-90, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-232198
6.
Karyotype analysis of qualified sperm donors on preliminary screening / 中华男科学杂志
National Journal of Andrology
; (12): 13-16, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-266220
7.
Chromosome copy analysis by single-cell comparative genomic hybridization technique based on primer extension preamplification and degenerate oligonucleotide primed-PCR / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 387-392, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-234399
8.
Identification of a cryptic 1p36.3 microdeletion in a patient with Prader-Willi-like syndrome features / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 524-529, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-234368
9.
Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 392-396, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-247309
10.
Cytogenetic study of 1780 cases of spontaneous abortion / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 258-260, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-813387
11.
Molecular cytogenetic analysis for a familial complex chromosomal rearrangement / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 302-304, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-321100
12.
Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 682-683, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-279969
13.
Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 608-610, 2004.
Artículo
en Zh
| WPRIM | ID: wpr-321184
14.
Molecular cytogenetic detection of partial chromosome 13q trisomy and its relation with the clinical features of tortilcollis / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 189-192, 2003.
Artículo
en Zh
| WPRIM | ID: wpr-248463
15.
Identification and characterization of marker chromosome in Turner syndrome / 中华妇产科杂志
Chinese Journal of Obstetrics and Gynecology
; (12)2000.
Artículo
en Zh
| WPRIM | ID: wpr-683406
Resultados
1 -
15
de 15
1
Próxima >
>>