Huang XL - Search Results

1

Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination.

Lebo RV, Milunsky J, Higgins AW, Loose B, Huang XL, Wyandt HE. Lebo RV, et al. Among authors: huang xl. Am J Med Genet. 1999 Aug 27;85(5):429-37. Am J Med Genet. 1999. PMID: 10405438

2

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.

Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A. Milunsky JM, et al. Among authors: huang xl. Am J Med Genet. 1996 Jan 22;61(3):269-73. doi: 10.1002/(SICI)1096-8628(19960122)61:3<269::AID-AJMG12>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8741873

3

Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.

Milunsky J, DeStefano AL, Huang XL, Baldwin CT, Michels VV, Jako G, Milunsky A. Milunsky J, et al. Among authors: huang xl. Am J Med Genet. 1997 Oct 3;72(1):66-70. doi: 10.1002/(sici)1096-8628(19971003)72:1<66::aid-ajmg14>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9295078

4

Schizophrenia susceptibility gene locus at Xp22.3.

Milunsky J, Huang XL, Wyandt HE, Milunsky A. Milunsky J, et al. Among authors: huang xl. Clin Genet. 1999 Jun;55(6):455-60. doi: 10.1034/j.1399-0004.1999.550610.x. Clin Genet. 1999. PMID: 10450863

5

46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.

Milunsky A, Huang X, Amos JA, Herskowitz J, Farrer LA, Wyandt HE. Milunsky A, et al. Am J Med Genet. 1993 Mar 1;45(5):589-93. doi: 10.1002/ajmg.1320450514. Am J Med Genet. 1993. PMID: 8096117

6

Further delineation of the critical region for the 9p-duplication syndrome.

Zou YS, Huang XL, Ito M, Newton S, Milunsky JM. Zou YS, et al. Among authors: huang xl. Am J Med Genet A. 2009 Feb;149A(2):272-6. doi: 10.1002/ajmg.a.32607. Am J Med Genet A. 2009. PMID: 19161157 No abstract available.

7

A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism.

Huang XL, Zou YS, Maher TA, Newton S, Milunsky JM. Huang XL, et al. Am J Med Genet A. 2010 Aug;152A(8):2112-4. doi: 10.1002/ajmg.a.33497. Am J Med Genet A. 2010. PMID: 20635338 No abstract available.

8

A locus for autosomal recessive achromatopsia on human chromosome 8q.

Milunsky A, Huang XL, Milunsky J, DeStefano A, Baldwin CT. Milunsky A, et al. Among authors: huang xl. Clin Genet. 1999 Jul;56(1):82-5. doi: 10.1034/j.1399-0004.1999.560112.x. Clin Genet. 1999. PMID: 10466422

9

Unmasking Kabuki syndrome: chromosome 8p22-8p23.1 duplication revealed by comparative genomic hybridization and BAC-FISH.

Milunsky JM, Huang XL. Milunsky JM, et al. Among authors: huang xl. Clin Genet. 2003 Dec;64(6):509-16. doi: 10.1046/j.1399-0004.2003.00189.x. Clin Genet. 2003. PMID: 14986831

10

Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.

Mark HF, Wyandt H, Huang XL, Milunsky JM. Mark HF, et al. Among authors: huang xl. Clin Genet. 2005 Aug;68(2):146-51. doi: 10.1111/j.1399-0004.2005.00466.x. Clin Genet. 2005. PMID: 15996211

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