Detalhe da pesquisa
1.
Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain.
Cell
; 151(3): 483-96, 2012 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-23101622
2.
A novel imprinted locus on bovine chromosome 18 homologous with human chromosome 16q24.1.
Mol Genet Genomics
; 299(1): 40, 2024 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38546894
3.
Contemporary Trends in Cardiac Surgical Care for Trisomy 13 and 18 Patients Admitted to Hospitals in the United States.
J Pediatr
; 268: 113955, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38340889
4.
[Genetic analysis of a case with mosaicism complex structural aberration of chromosome 18].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(1): 101-105, 2024 Jan 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-38171568
5.
The Consequences of Abnormal Gene Dosage: Lessons from Chromosome 18.
Trends Genet
; 36(10): 764-776, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32660784
6.
The molecular mechanisms of recombinant chromosome 18 with parental pericentric inversions and a review of the literature.
J Hum Genet
; 68(9): 625-634, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37161033
7.
Chromosome 18 Loss of Heterozygosity in Small Intestinal Neuroendocrine Tumours: Multi-Omic and Tumour Composition Analyses.
Neuroendocrinology
; 113(9): 915-923, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36907174
8.
[Genetic analysis of a Chinese pedigree with 18q21.2-q22.3 duplication and deletion in two offspring respectively resulting from a maternal intrachromosomal insertion].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(4): 483-489, 2023 Apr 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-36972947
9.
Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes.
Hum Mol Genet
; 29(2): 238-247, 2020 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31813999
10.
Perinatal Outcomes of Fetuses and Infants Diagnosed with Trisomy 13 or Trisomy 18.
J Pediatr
; 247: 116-123.e5, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35452657
11.
Hematological and Genetic Markers in the Rational Approach to Patients With HCV Sustained Virological Response With or Without Persisting Cryoglobulinemic Vasculitis.
Hepatology
; 74(3): 1164-1173, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33721342
12.
A case report of Ring chromosome 18 with systemic Lupus Erythematosus and Crohn's disease.
Mol Biol Rep
; 49(2): 1085-1088, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34775554
13.
Pulmonary artery sling in a 22-month-old boy with 18q deletion syndrome: A rare but possible association.
Echocardiography
; 39(5): 741-744, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35434845
14.
Karyotype patterns, clinical features, and parental ages of three predominant live born autosomal trisomies of Northeast Malaysia.
Malays J Pathol
; 44(2): 235-244, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-36043586
15.
The diagnostic and therapeutic challenges of Grade 3B follicular lymphoma.
Br J Haematol
; 195(1): 15-24, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704790
16.
The Ligon lintless -2 Short Fiber Mutation Is Located within a Terminal Deletion of Chromosome 18 in Cotton.
Plant Physiol
; 183(1): 277-288, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32102829
17.
A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocation.
Am J Med Genet A
; 185(5): 1532-1537, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33569883
18.
Surveillance guidelines for children with trisomy 18.
Am J Med Genet A
; 185(4): 1294-1303, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33527722
19.
Interdisciplinary care of children with trisomy 13 and 18.
Am J Med Genet A
; 185(3): 966-977, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33381915
20.
Genetic variants and functional pathways associated with resilience to Alzheimer's disease.
Brain
; 143(8): 2561-2575, 2020 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32844198