Detalhe da pesquisa
1.
Increased genome size is caused by heterochromatin addition in two non-related bat species, Hesperoptenus doriae and Philetor brachypterus (Vespertilionidae, Chiroptera, Mammalia).
Chromosoma
; 132(4): 269-288, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37322170
2.
Refined cytogenetic IPSS-R evaluation by the use of SNP array in a cohort of 290 MDS patients.
Genes Chromosomes Cancer
; 62(12): 721-731, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37449676
3.
Cytogenetic characterization and karyotype evolution in six Macroptilium species (Leguminosae).
Genome
; 66(7): 165-174, 2023 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37094381
4.
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing.
Genes Chromosomes Cancer
; 61(1): 22-26, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34460133
5.
[Phenotypic and genetic analysis of a child with partial trisomy 7q].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(5): 604-608, 2023 May 10.
Artigo
em Zh
| MEDLINE | ID: mdl-37102298
6.
[Comparison of detection rates of chromosome G-banding karyotype analysis and fluorescence in situ hybridization among children with sex chromosome mosaicisms].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(1): 12-16, 2023 Jan 10.
Artigo
em Zh
| MEDLINE | ID: mdl-36584993
7.
[Prenatal diagnosis and genetic analysis of a rare case with 8p deletion and duplication].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(1): 96-100, 2023 Jan 10.
Artigo
em Zh
| MEDLINE | ID: mdl-36585010
8.
Prognostic heterogeneity of adult B-cell precursor acute lymphoblastic leukaemia patients with t(1;19)(q23;p13)/TCF3-PBX1 treated with measurable residual disease-oriented protocols.
Br J Haematol
; 196(3): 670-675, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34549416
9.
Chromosome banding analysis and genomic microarrays are both useful but not equivalent methods for genomic complexity risk stratification in chronic lymphocytic leukemia patients.
Haematologica
; 107(3): 593-603, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33691382
10.
Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia.
J Med Genet
; 58(10): 679-686, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32900840
11.
[Clinical and genetic analysis of a patient with 10q26.3 microdeletion in conjunct with 18q22.3q23 microduplication].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(12): 1415-1418, 2022 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-36453971
12.
[Genetic analysis of a case with 2q37 microdeletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(1): 81-84, 2022 Jan 10.
Artigo
em Zh
| MEDLINE | ID: mdl-34964974
13.
[Genetic analysis and prenatal diagnosis of a fetus with Xq25 microduplication].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(4): 425-427, 2022 Apr 10.
Artigo
em Zh
| MEDLINE | ID: mdl-35446981
14.
[Clinical genetic analysis of an infant with 1q21.3-qter duplication and Xpter-p11 deletion caused by maternal balanced chromosomal translocation].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(5): 514-517, 2022 May 10.
Artigo
em Zh
| MEDLINE | ID: mdl-35598268
15.
[Genetic analysis of an infant with rare type of trisomy 21 syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(6): 634-636, 2022 Jun 10.
Artigo
em Zh
| MEDLINE | ID: mdl-35773770
16.
[Genetic analysis of a child with Pitt-Hopkins syndrome due to a 18q21.2q21.32 deletion].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(10): 1149-1152, 2022 Oct 10.
Artigo
em Zh
| MEDLINE | ID: mdl-36184102
17.
[A rare case of dicentric ring chromosome and derivative ring chromosome Chimera].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(5): 534-536, 2022 May 10.
Artigo
em Zh
| MEDLINE | ID: mdl-35598273
18.
Faint gray bands in Drosophila melanogaster polytene chromosomes are formed by coding sequences of housekeeping genes.
Chromosoma
; 129(1): 25-44, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31820086
19.
Clinical Features of de novo Pure 16q21q24.1 Chromosome Duplication.
Cytogenet Genome Res
; 161(3-4): 160-166, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34107486
20.
SINE-B1 Distribution and Chromosome Rearrangements in the South American Proechimys gr. goeldii (Echimyidae, Rodentia).
Cytogenet Genome Res
; 161(1-2): 6-13, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33556945