The Global State of the Genetic Counseling Profession
Abacan, MaryAnn, Alsubaie, Lamia, Barlow-Stewart, Kristine, Caanen, Beppy, Cordier, Christophe, Courtney, Eliza, Davoine, Emeline, Edwards, Janice, Elackatt, Niby J, Gardiner, Kate, Guan, Yue, Huang, Lian-Hua, Malmgren, Charlotta Ingvoldstad, Kejriwal, Sahil, Kim, Hyon J, Lambert, Deborah, Lantigua-Cruz, Paulina Araceli, Lee, Juliana M H, Lodahl, Marianne, Lunde, Åshild, Macaulay, Shelley, Macciocca, Ivan, Margarit, Sonia, Middleton, Anna, Moldovan, Ramona, Ngeow, Joanne, Obregon-Tito, Alexandra J, Ormond, Kelly E, Paneque, Milena, Powell, Karen, Sanghavi, Kunal, Scotcher, Diana, Scott, Jenna, Juhé, Clara Serra, Shkedi-Rafid, Shiri, Wessels, Tina-Marié, Yoon, Sook-Yee, Wicklund, Catherine
Published in European journal of human genetics : EJHG (01.02.2019)
Published in European journal of human genetics : EJHG (01.02.2019)
Get full text
Journal Article
Distinct regulation of the anterior and posterior myeloperoxidase expression by Etv2 and Gata1 during primitive Granulopoiesis in zebrafish
Glenn, Nicole O., Schumacher, Jennifer A., Kim, Hyon J., Zhao, Emma J., Skerniskyte, Jurate, Sumanas, Saulius
Published in Developmental biology (01.09.2014)
Published in Developmental biology (01.09.2014)
Get full text
Journal Article
Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases
Park, Sang-Jin, Jung, Eun Hye, Ryu, Ran-Suk, Kang, Hyun Woong, Ko, Jung-Min, Kim, Hyon J, Cheon, Chong Kun, Hwang, Sang-Hyun, Kang, Ho-Young
Published in Molecular cytogenetics (09.05.2011)
Published in Molecular cytogenetics (09.05.2011)
Get full text
Journal Article
Identifying the KAT6B Mutation via Diagnostic Exome Sequencing to Diagnose Say-Barber-Biesecker-Young-Simpson Syndrome in Three Generations of a Family
Kim, Yong Rok, Park, Jong Bum, Lee, Yung Jin, Hong, Mi Jin, Kim, Hyeong Tae, Kim, Hyon J
Published in Annals of rehabilitation medicine (01.06.2017)
Published in Annals of rehabilitation medicine (01.06.2017)
Get full text
Journal Article
Wnt5 signaling in vertebrate pancreas development
Kim, Hyon J, Schleiffarth, Jack R, Jessurun, Jose, Sumanas, Saulius, Petryk, Anna, Lin, Shuo, Ekker, Stephen C
Published in BMC biology (24.10.2005)
Published in BMC biology (24.10.2005)
Get full text
Journal Article
Inhibition of Bcl-xL by ABT-737 enhances chemotherapy sensitivity in neurofibromatosis type 1-associated malignant peripheral nerve sheath tumor cells
LEE, SU-JIN, PARK, HO-JIN, KIM, YOUNG-HWA, KIM, BO-YOUNG, JIN, HYUN-SEOK, KIM, HYON J, HAN, JAE-HO, YIM, HYUNEE, JEONG, SEON-YONG
Published in International journal of molecular medicine (01.08.2012)
Published in International journal of molecular medicine (01.08.2012)
Get full text
Journal Article
A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome
Jeong, Seon-Yong, Kim, Bo-Young, Kim, Hyon J, Yang, Jeong-A, Kim, Ok-Hwa
Published in Journal of human genetics (01.11.2010)
Published in Journal of human genetics (01.11.2010)
Get full text
Journal Article
Genetic Analysis of Early Endocrine Pancreas Formation in Zebrafish
Kim, Hyon J, Sumanas, Saulius, Palencia-Desai, Sharina, Dong, Yuan, Chen, Jau-Nien, Lin, Shuo
Published in Molecular endocrinology (Baltimore, Md.) (01.01.2006)
Published in Molecular endocrinology (Baltimore, Md.) (01.01.2006)
Get full text
Journal Article
A case of Birt-Hogg-Dubé syndrome
Kim, En Hyung, Jeong, Seon-Yong, Kim, Hyon J, Kim, You Chan
Published in Journal of Korean medical science (01.04.2008)
Published in Journal of Korean medical science (01.04.2008)
Get full text
Journal Article
Strabismus and poor stereoacuity associated with Kabuki syndrome
Kim, Nam Gil, Kim, Hyon J, Hwang, Jeong-Min
Published in Korean journal of ophthalmology (01.04.2011)
Published in Korean journal of ophthalmology (01.04.2011)
Get full text
Journal Article
Fragile X syndrome in Korea: a case series and a review of the literature
Yim, Shin-Young, Jeon, Bo Hyun, Yang, Jung A, Kim, Hyon J
Published in Journal of Korean medical science (01.06.2008)
Published in Journal of Korean medical science (01.06.2008)
Get full text
Journal Article
A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion
Kim, Hyo Jeong, Cho, Eunhae, Park, Jong Bum, Im, Woo Young, Kim, Hyon J
Published in European journal of medical genetics (01.02.2015)
Published in European journal of medical genetics (01.02.2015)
Get full text
Journal Article
Phenotypic Analysis of Korean Patients with Abnormal Chromosomal Microarray in Patients with Unexplained Developmental Delay/Intellectual Disability
Kim, Hyo Jeong, Park, Chang Il, Lim, Jae Woo, Lee, Gyung Min, Cho, Eunhae, Kim, Hyon J
Published in Yonsei medical journal (01.05.2018)
Published in Yonsei medical journal (01.05.2018)
Get full text
Journal Article
Clinical and genetic characteristics of Korean patients with Gaucher disease
Jeong, Seon-Yong, Park, Sang-Jin, Kim, Hyon J.
Published in Blood cells, molecules, & diseases (15.01.2011)
Published in Blood cells, molecules, & diseases (15.01.2011)
Get full text
Journal Article
분자유전검사로 확진된 한국인 고셔병 환자의 눈 이상
이상문, Sangmoon Lee, 김현주, Hyon J Kim, 정선용, Seon Yong Jeong, 황정민, Jeong Min Hwang
Published in Daihan angwa haghoi jabji (15.01.2013)
Get full text
Published in Daihan angwa haghoi jabji (15.01.2013)
Journal Article