Genetic approaches to understanding the causes of stuttering

por Drayna, Dennis, Kang, Changsoo
Publicado 2011

Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation

por Fedyna, Alison, Drayna, Dennis, Kang, Changsoo
Publicado 2010

A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans

por Cha, Seongwon, Park, Ah Yeon, Kang, Changsoo
Publicado 2015

Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCR

por Chang, Mun Young, Kim, Ah Reum, Kim, Min Young, Kim, Soyoung, Yoon, Jinsun, Han, Jae Joon, Ahn, Soyeon, Kang, Changsoo, Choi, Byung Yoon
Publicado 2016

Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14

por Pastore, Stephen F., Muhammad, Tahir, Harripaul, Ricardo, Lau, Rebecca, Khan, Muhammad Tariq Masood, Khan, Muhammad Ismail, Islam, Omar, Kang, Changsoo, Ayub, Muhammad, Jelani, Musharraf, Vincent, John B.
Publicado 2021

One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR

por Chang, Mun Young, Ahn, Soyeon, Kim, Min Young, Han, Jin Hee, Park, Hye-Rim, Seo, Han Kyu, Yoon, Jinsun, Lee, Seungmin, Oh, Doo-Yi, Kang, Changsoo, Choi, Byung Yoon
Publicado 2018

A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalities

por Jelani, Musharraf, Dooley, Hannah C., Gubas, Andrea, Mohamoud, Hussein Sheikh Ali, Khan, Muhammad Tariq Masood, Ali, Zahir, Kang, Changsoo, Rahim, Fazal, Jan, Amin, Vadgama, Nirmal, Khan, Muhammad Ismail, Al-Aama, Jumana Yousuf, Khan, Asifullah, Tooze, Sharon A, Nasir, Jamal
Publicado 2019