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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
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.
Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM. Wyandt HE, et al. Among authors: huang xl. Exp Mol Pathol. 2006 Jun;80(3):262-6. doi: 10.1016/j.yexmp.2005.12.008. Epub 2006 Mar 6. Exp Mol Pathol. 2006. PMID: 16516886
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
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
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
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
Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).
Milunsky J, Huang XL, Baldwin CT, Farah MG, Milunsky A. Milunsky J, et al. Among authors: huang xl. Cancer Genet Cytogenet. 1998 Oct 15;106(2):173-6. doi: 10.1016/s0165-4608(98)00063-6. Cancer Genet Cytogenet. 1998. PMID: 9797786
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
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
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