Works by Seong, M‐W

Results: 9

Clinical applications of next-generation sequencing-based gene panel in patients with muscular dystrophy: Korean experience.

Published in:

Clinical Genetics, 2016, v. 89, n. 4, p. 484, doi. 10.1111/cge.12621

By:

Seong, M.‐W.;
Cho, A.;
Park, H.W.;
Seo, S.H.;
Lim, B.C.;
Seol, D.;
Cho, S.I.;
Park, S.S.;
Chae, J.H.

Publication type:

Article

Identification of novel mutations in the VPS33B gene involved in arthrogryposis, renal dysfunction, and cholestasis syndrome.

Published in:

Clinical Genetics, 2015, v. 88, n. 1, p. 80, doi. 10.1111/cge.12442

By:

Seo, S. H.;
Hwang, S. M.;
Ko, J. M.;
Ko, J. S.;
Hyun, Y. J.;
Cho, S. I.;
Park, H.;
Kim, S. Y.;
Seong, M.‐W.;
Park, S. S.

Publication type:

Article

Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea.

Published in:

Clinical Genetics, 2014, v. 86, n. 5, p. 482, doi. 10.1111/cge.12304

By:

Kim, J.H.;
Seong, M.‐W.;
Lee, K.E.;
Choi, H.J.;
Ku, E.J.;
Bae, J.H.;
Park, S.S.;
Choi, S.H.;
Kim, S.W.;
Shin, CS;
Kim, S.Y.

Publication type:

Article

Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis.

Published in:

Clinical Genetics, 2013, v. 83, n. 5, p. 494, doi. 10.1111/j.1399-0004.2012.01954.x

By:

Seo, SH;
Ahn, HS;
Yu, YS;
Kang, HJ;
Park, KD;
Cho, SI;
Park, JS;
Hyun, YJ;
Kim, JY;
Seong, M‐W;
Park, SS

Publication type:

Article

Phase analysis identifies compound heterozygous deletions of the PARK2 gene in patients with early-onset Parkinson disease.

Published in:

Clinical Genetics, 2012, v. 82, n. 1, p. 77, doi. 10.1111/j.1399-0004.2011.01693.x

By:

Kim, S Y;
Seong, M W;
Jeon, B S;
Ko, H S;
Kim, J Y;
Park, S S

Publication type:

Article

Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation.

Published in:

Clinical Genetics, 2009, v. 76, n. 2, p. 152, doi. 10.1111/j.1399-0004.2009.01202.x

By:

Seong, M.-W.;
Cho, S. I.;
Noh, D.-Y.;
Han, W.;
Kim, S.-W.;
Park, C.-M.;
Park, H.-W.;
Kim, S. Y.;
Kim, J. Y.;
Park, S. S.

Publication type:

Article

The etiology of genetic neonatal/infantile cholestasis and usefulness of the molecular genetic testing.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 2022, v. 74, p. 764, doi. 10.1097/MPG.0000000000003446

By:

Hahn, J. W.;
Moon, S. Y.;
Shin, M.;
Seong, M. W.;
Park, S. S.;
Moon, J. S.;
Ko, J. S.

Publication type:

Article

PKHD1 mutations and clinical manifestations in children with Caroli syndrome and autosomal recessive polycystic kidney disease.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 2022, v. 74, p. 709, doi. 10.1097/MPG.0000000000003446

By:

Moon, S. Y.;
Hahn, J. W.;
Shin, M.;
Seong, M.-W.;
Park, S. S.;
Moon, J. S.;
Cheong, H. i.;
Ko, J. S.

Publication type:

Article

Diagnosis and treatment of nail melanoma: a review of the clinicopathologic, dermoscopic, and genetic characteristics.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 5, p. 651, doi. 10.1111/jdv.17975

By:

Darmawan, C.C.;
Ohn, J.;
Mun, J.‐H.;
Kim, S.;
Lim, Y.;
Jo, S.J.;
Kim, Y.‐g.;
Kim, B.;
Seong, M.‐W.;
Kim, B.J.;
Lee, C.;
Kwak, Y.;
Chung, H.J.;
Virós, A.;
Lee, D.Y.

Publication type:

Article