Detalles de la búsqueda
1.
A DMD case caused by X chromosome rearrangement.
Yi Chuan
; 45(1): 88-95, 2023 Jan 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-36927641
2.
Pronuclear removal of tripronuclear zygotes can establish heteroparental normal karyotypic human embryonic stem cells.
J Assist Reprod Genet
; 33(2): 255-63, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26727933
3.
Trace levels of mitomycin C disrupt genomic integrity and lead to DNA damage response defect in long-term-cultured human embryonic stem cells.
Arch Toxicol
; 89(1): 33-45, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24838295
4.
Karyotype determination and reproductive guidance for short stature women with a hidden Y chromosome fragment.
Reprod Biomed Online
; 27(1): 89-95, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23664816
5.
[A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(1): 87-90, 2013 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-23450488
6.
Defects in phospholipase C zeta cause polyspermy and low fertilization after conventional IVF: not just ICSI failure.
Asian J Androl
; 2023 Nov 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-38048167
7.
One healthy live birth after preimplantation genetic testing of a cryptic balanced translocation (9;13) in a family with cerebral palsy and glaucoma: a case report.
BMC Med Genomics
; 14(1): 82, 2021 03 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-33731094
8.
[Chromosome copy analysis by single-cell comparative genomic hybridization technique based on primer extension preamplification and degenerate oligonucleotide primed-PCR].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 27(4): 387-92, 2010 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-20677142
9.
[Identification of a cryptic 1p36.3 microdeletion in a patient with Prader-Willi-like syndrome features].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 27(5): 524-9, 2010 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-20931530
10.
Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies.
Mol Cytogenet
; 13: 15, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32391085
11.
Tumor progression of culture-adapted human embryonic stem cells during long-term culture.
Genes Chromosomes Cancer
; 47(8): 665-79, 2008 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-18470900
12.
Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby.
J Assist Reprod Genet
; 29(11): 1299-304, 2012 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-23001237
13.
[Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 24(4): 392-6, 2007 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-17680527
14.
[Identification and characterization of marker chromosome in Turner syndrome].
Zhonghua Fu Chan Ke Za Zhi
; 42(10): 679-82, 2007 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-18241543
15.
[Advance in mutation analysis of the candidate genes in premature ovarian failure].
Yi Chuan
; 28(11): 1467-71, 2006 Nov.
Artículo
en Zh
| MEDLINE | ID: mdl-17098720
16.
The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes.
Mol Cytogenet
; 7(1): 64, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-25324898
17.
Mutation Analysis and Prenatal Exclusion of Fibrodysplasia Ossificans Progressiva in a Chinese Fetus.
Genet Test Mol Biomarkers
; 2010 Jan 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-20059392
18.
Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.
Fertil Steril
; 92(2): 828.e3-6, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19524892
Resultados
1 -
18
de 18
1
Próxima >
>>