Huang XL - Search Results

1

[Application of fluorescence in situ hybridization in prenatal diagnosis of complex chromosomal abnormalities].

Shen YY, Li J, Kong H, Wu HN, Wu Q, Ge YS, Huang XL, Zhou YL. Shen YY, et al. Among authors: huang xl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):529-32. doi: 10.3760/cma.j.issn.1003-9406.2009.05.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806574 Chinese.

2

[Molecular and cytogenetic study on 18 cases of amenorrhea: the use of fluorescence in situ hybridization and high resolution-comparative genomic hybridization].

Kong H, Ge YS, Wu Q, Wu HN, Zhou DX, Shen YY, Zheng YL, Cai MJ, Li J, Huang XL. Kong H, et al. Among authors: huang xl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Jun;24(3):256-60. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17557232 Chinese.

3

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

4

Correlation of abnormal rapid FISH and chromosome results from amniocytes for prenatal diagnosis.

Wyandt HE, Tonk VS, Huang XL, Evans AT, Milunsky JM, Milunsky A. Wyandt HE, et al. Among authors: huang xl. Fetal Diagn Ther. 2006;21(2):235-40. doi: 10.1159/000089310. Fetal Diagn Ther. 2006. PMID: 16491010 Clinical Trial.

5

Prenatal and postnatal characterization of a de novo Xq22.1 terminal deletion.

Vaglio A, Greif G, Bernal M, Sanguinetti C, Mechoso B, Quadrelli A, Tucci P, Milunsky JM, Huang XL, Pagano S, Quadrelli R. Vaglio A, et al. Among authors: huang xl. Genet Test. 2006 Winter;10(4):272-6. doi: 10.1089/gte.2006.10.272. Genet Test. 2006. PMID: 17253933

6

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.

Vaglio A, Milunsky A, Huang XL, Quadrelli A, Mechoso B, Maher TA, Quadrelli R. Vaglio A, et al. Among authors: huang xl. Eur J Med Genet. 2008 Jul-Aug;51(4):332-42. doi: 10.1016/j.ejmg.2008.01.001. Epub 2008 Jan 25. Eur J Med Genet. 2008. PMID: 18316257

7

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

8

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

9

A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.

Mechoso B, Vaglio A, Quadrelli A, Mark HF, Huang XL, Milunsky A, Quadrelli R. Mechoso B, et al. Among authors: huang xl. Fetal Diagn Ther. 2007;22(4):249-53. doi: 10.1159/000100784. Epub 2007 Mar 16. Fetal Diagn Ther. 2007. PMID: 17369689

10

Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomy.

Thomas FP, Geller TJ, Hahn AF, Gutmann L, Huang XL, Wu H, Wyandt HE, Lebo RV. Thomas FP, et al. Among authors: huang xl. Ann N Y Acad Sci. 1999 Sep 14;883:472-6. Ann N Y Acad Sci. 1999. PMID: 10586277 No abstract available.

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