Detalhe da pesquisa
1.
The Thai reference exome (T-REx) variant database.
Clin Genet
; 100(6): 703-712, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34496037
2.
The association of obesity and coronary artery disease genes with response to SSRIs treatment in major depression.
J Neural Transm (Vienna)
; 126(1): 35-45, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30610379
3.
A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature.
Cytogenet Genome Res
; 144(1): 1-8, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25171325
4.
PTPRF is disrupted in a patient with syndromic amastia.
BMC Med Genet
; 12: 46, 2011 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-21453473
5.
Bilateral squamosal synostosis: unusual presentation of chromosome 1p12-1p13.3 deletion. Illustrative case.
J Neurosurg Case Lessons
; 1(3): CASE20102, 2021 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36034505
6.
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.
Front Psychiatry
; 9: 65, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29559929
7.
Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual Disabilities.
Genet Res Int
; 2016: 9153740, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27822388
8.
Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure.
PLoS One
; 8(11): e79522, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24223962
9.
Effect of the N-terminal sequence on the binding affinity of transthyretin for human retinol-binding protein.
FEBS J
; 278(18): 3337-47, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21777382
10.
Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q.
Eur J Hum Genet
; 18(12): 1310-4, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20648051
11.
Prenatal exclusion of subtelomeric deletion 1p by fluorescent in situ hybridization.
Arch Gynecol Obstet
; 275(4): 237-40, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16983561
12.
Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletion.
Am J Med Genet A
; 140(23): 2598-602, 2006 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17001671
13.
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome.
Am J Med Genet A
; 130A(2): 181-90, 2004 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15372530
14.
Tetralogy of Fallot with absent pulmonary valve in a de novo derivative chromosome 9 with duplication of 9p13 --> 9pter and deletion of 9q34.3.
Am J Med Genet A
; 140(18): 1981-7, 2006 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16906562