Chariyawan Charalsawadi

发表

Mosaicism for trisomy 21: A review

C. Jackson-Cook, P. Papavassiliou, Chariyawan Charalsawadi, 2015, American journal of medical genetics. Part A.

Estimates of the Frequency of Mosaicism in People Diagnosed With Down Syndrome

C. Jackson-Cook, P. Papavassiliou, Chariyawan Charalsawadi, 2014 .

No Evidence of Abnormal Expression of Beta-Catenin and Bcl-2 Proteins in Pilomatricoma as One Clinical Feature of Tetrasomy 9p Syndrome

P. Limprasert, Kanoot Jaruthamsophon, Chariyawan Charalsawadi, 2021, International Journal of Pediatrics.

Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study

S. Mahasirimongkol, Chariyawan Charalsawadi, N. Nakwan, 2021, Jornal de pediatria.

Clinical delineation of 18q11‐q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects

K. Rojnueangnit, A. Novelli, N. Jinawath, 2019, Molecular genetics & genomic medicine.

Case Report: An Atypical Angelman Syndrome Case With Obesity and Fulfilled Autism Spectrum Disorder Identified by Microarray

P. Limprasert, Areerat Hnoonual, Chariyawan Charalsawadi, 2021, Frontiers in Genetics.

A Case with a Ring Chromosome 13 in a Cohort of 203 Children with Non-Syndromic Autism and Review of the Cytogenetic Literature

V. Praphanphoj, P. Limprasert, Rawiwan Roongpraiwan, 2014, Cytogenetic and Genome Research.

Mosaicism for trisomy21: Utility of array-based technology for its detection and its influence on telomere length and the frequency of acquired chromosome abnormalities

Chariyawan Charalsawadi, 2011 .

Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature

P. Limprasert, N. Jinawath, Areerat Hnoonual, 2022, Frontiers in Genetics.

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

V. Praphanphoj, P. Limprasert, Chariyawan Charalsawadi, 2016, Genetics research international.

Maternal Age-Specific Rates for Trisomy 21 and Common Autosomal Trisomies in Fetuses from a Single Diagnostic Center in Thailand

H. Sriplung, P. Limprasert, Kanoot Jaruthamsophon, 2016, PloS one.

Two case reports of chromosomal abnormalities using Fluorescence In Situ Hybridization (FISH)

P. Limprasert, Chariyawan Charalsawadi, S. Jaruratanasirikul, 2004 .

Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.

P. Limprasert, Chariyawan Charalsawadi, T. Sripo, 2005, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Common Clinical Characteristics and Rare Medical Problems of Fragile X Syndrome in Thai Patients and Review of the Literature

A. Geater, P. Limprasert, Chariyawan Charalsawadi, 2017, International journal of pediatrics.

Molecular analysis of uniparental disomy in a Thai patient with Prader-Willi syndrome

P. Limprasert, Sinitdhorn Rujirabanjerd, Chariyawan Charalsawadi, 2005 .

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

V. Praphanphoj, P. Limprasert, Chariyawan Charalsawadi, 2016, Genetics research international.

Molecular identification of HLA‐B75 serotype markers by qPCR: A more inclusive pharmacogenetic approach before carbamazepine prescription

Kanoot Jaruthamsophon, Areerat Hnoonual, Chariyawan Charalsawadi, 2024, Clinical and translational science.