Jung JH - Search Results

1

Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.

Fan YS, Siu VM, Jung JH, Farrell SA, Côté GB. Fan YS, et al. Among authors: jung jh. Am J Med Genet. 2001 Oct 15;103(3):231-4. doi: 10.1002/ajmg.1534.abs. Am J Med Genet. 2001. PMID: 11745996

2

18q-mosaicism associated with Rett syndrome phenotype.

Gordon K, Siu VM, Sergovich F, Jung J. Gordon K, et al. Am J Med Genet. 1993 Apr 15;46(2):142-4. doi: 10.1002/ajmg.1320460208. Am J Med Genet. 1993. PMID: 8484399

3

Choroideremia associated with an X-autosomal translocation.

Siu VM, Gonder JR, Jung JH, Sergovich FR, Flintoff WF. Siu VM, et al. Among authors: jung jh. Hum Genet. 1990 Apr;84(5):459-64. doi: 10.1007/BF00195820. Hum Genet. 1990. PMID: 2323779 Free PMC article.

4

Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements.

Fan YS, Siu VM, Jung JH, Xu J. Fan YS, et al. Among authors: jung jh. Genet Test. 2000;4(1):9-14. doi: 10.1089/109065700316417. Genet Test. 2000. PMID: 10794355

5

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes.

Fan YS, Zhang Y, Speevak M, Farrell S, Jung JH, Siu VM. Fan YS, et al. Among authors: jung jh. Genet Med. 2001 Nov-Dec;3(6):416-21. doi: 10.1097/00125817-200111000-00007. Genet Med. 2001. PMID: 11715006 Free article.

6

Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years.

Fan YS, Jung J, Hamilton B. Fan YS, et al. Am J Med Genet. 1999 Sep 10;86(2):118-23. doi: 10.1002/(sici)1096-8628(19990910)86:2<118::aid-ajmg6>3.0.co;2-s. Am J Med Genet. 1999. PMID: 10449645

7

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.

Lowther C, Speevak M, Armour CM, Goh ES, Graham GE, Li C, Zeesman S, Nowaczyk MJ, Schultz LA, Morra A, Nicolson R, Bikangaga P, Samdup D, Zaazou M, Boyd K, Jung JH, Siu V, Rajguru M, Goobie S, Tarnopolsky MA, Prasad C, Dick PT, Hussain AS, Walinga M, Reijenga RG, Gazzellone M, Lionel AC, Marshall CR, Scherer SW, Stavropoulos DJ, McCready E, Bassett AS. Lowther C, et al. Among authors: jung jh. Genet Med. 2017 Jan;19(1):53-61. doi: 10.1038/gim.2016.54. Epub 2016 May 19. Genet Med. 2017. PMID: 27195815 Free PMC article.

8

Genetic analysis of patients with the Saethre-Chotzen phenotype.

Chun K, Teebi AS, Jung JH, Kennedy S, Laframboise R, Meschino WS, Nakabayashi K, Scherer SW, Ray PN, Teshima I. Chun K, et al. Among authors: jung jh. Am J Med Genet. 2002 Jun 15;110(2):136-43. doi: 10.1002/ajmg.10400. Am J Med Genet. 2002. PMID: 12116251

9

A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkage.

Rodenhiser DI, Coulter-Mackie MB, Jung JH, Singh SM. Rodenhiser DI, et al. Among authors: jung jh. J Med Genet. 1991 Nov;28(11):746-51. doi: 10.1136/jmg.28.11.746. J Med Genet. 1991. PMID: 1685193 Free PMC article.

10

A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.

Rodenhiser DI, Ainsworth PJ, Coulter-Mackie MB, Singh SM, Jung JH. Rodenhiser DI, et al. Among authors: jung jh. J Med Genet. 1993 May;30(5):363-8. doi: 10.1136/jmg.30.5.363. J Med Genet. 1993. PMID: 8320697 Free PMC article.

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