| 33314840 | [Characteristics and driving forces of wetland landscape pattern evolution of the city belt along the Yellow River in Ningxia, China]. | Ying Yong Sheng Tai Xue Bao | 2020 |
| 26575889 | [Clinical and pathological characteristics and prognosis of children with histiocytic necrotizing lymphadenitis]. | Zhongguo Dang Dai Er Ke Za Zhi | 2015 |
| 21130848 | Distribution of retinoic acid receptor-α immunoreactivity in the human hypothalamus. | Neuroscience | 2011 |
| 21664419 | Stress and glucocorticoids regulated corticotropin releasing factor in rat prefrontal cortex. | Mol Cell Endocrinol | 2011 |
| 20659790 | Chronic all-trans retinoic acid administration induced hyperactivity of HPA axis and behavioral changes in young rats. | Eur Neuropsychopharmacol | 2010 |
| 19282872 | William's syndrome: gene expression is related to parental origin and regional coordinate control. | J Hum Genet | 2009 |
| 19597142 | The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies. | Proc Natl Acad Sci U S A | 2009 |
| 19596122 | The involvement of retinoic acid receptor-alpha in corticotropin-releasing hormone gene expression and affective disorders. | Biol Psychiatry | 2009 |
| 19356693 | Distribution of acid-sensing ion channel 3 in the rat hypothalamus. | Neuroscience | 2009 |
| 19205026 | Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays. | Am J Med Genet A | 2009 |
| 18597742 | Estrogen receptor-alpha and -beta regulate the human corticotropin-releasing hormone gene through similar pathways. | Brain Res | 2008 |
| 16418593 | Deletion of chromosome 21 disturbs human brain morphogenesis. | Genet Med | 2006 |
| 15952108 | Detection of chromosome aberrations in Chinese children with autism using G-banding and BAC FISH. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2005 |
| 15020820 | BAC mapping using fluorescence in situ hybridization. | Methods Mol Biol | 2004 |
| 12865760 | Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. | Genet Med | 2003 |
| 12909340 | The 200-kb segmental duplication on human chromosome 21 originates from a pericentromeric dissemination involving human chromosomes 2, 18 and 13. | Gene | 2003 |
| 12697057 | Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1. | BMC Genomics | 2003 |
| 12051741 | Mammalian DSCAMs: roles in the development of the spinal cord, cortex, and cerebellum? | Biochem Biophys Res Commun | 2002 |
| 12397812 | BAC resource for molecular cytogenetics. | Methods Mol Biol | 2002 |
| 11977162 | Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome. | Am J Med Genet | 2002 |
| 11576731 | Towards a full karyotype screening of interphase cells: 'FISH and chip' technology. | Mol Cell Endocrinol | 2001 |
| 11280950 | Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel. | Genet Med | 2001 |
| 11280955 | Down syndrome congenital heart disease: a narrowed region and a candidate gene. | Genet Med | 2001 |
| 11237021 | Integration of cytogenetic landmarks into the draft sequence of the human genome. | Nature | 2001 |
| 11237014 | A physical map of the human genome. | Nature | 2001 |
| 11353394 | A triple color FISH technique for mouse chromosome identification. | Mamm Genome | 2001 |
| 11304567 | Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies. | Lab Invest | 2001 |
| 11283799 | Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans. | Am J Hum Genet | 2001 |
| 11015462 | Partial tetrasomy 21 in a male infant. | J Med Genet | 2000 |
| 10861662 | Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12). | Am J Med Genet | 2000 |
| 10953236 | VI. Genome structure and cognitive map of Williams syndrome. | J Cogn Neurosci | 2000 |
| 10938284 | The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity. | J Biol Chem | 2000 |
| 10523528 | Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. | Genome Res | 1999 |
| 10405324 | A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24. | Biochem Biophys Res Commun | 1999 |
| 10438519 | Involvement of protein kinase Cepsilon (PKCepsilon) in thyroid cell death. A truncated chimeric PKCepsilon cloned from a thyroid cancer cell line protects thyroid cells from apoptosis. | J Biol Chem | 1999 |
| 10330132 | Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps. | Genome Res | 1999 |
| 10191094 | Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA. | Genomics | 1999 |
| 10636446 | FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome. | Clin Genet | 1999 |
| 9683604 | From amplification to gene in thyroid cancer: a high-resolution mapped bacterial-artificial-chromosome resource for cancer chromosome aberrations guides gene discovery after comparative genome hybridization. | Am J Hum Genet | 1998 |
| 9426258 | DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system. | Hum Mol Genet | 1998 |
| 10072586 | Assignment of the GOV (Glioblastoma overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization. | Cytogenet Cell Genet | 1998 |
| 9675132 | JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24. | Biochem Biophys Res Commun | 1998 |
| 9344663 | The structure and chromosome location of the human chondroadherin gene (CHAD). | Genomics | 1997 |
| 9169140 | Molecular characterization of human neogenin, a DCC-related protein, and the mapping of its gene (NEO1) to chromosomal position 15q22.3-q23. | Genomics | 1997 |
| 9110173 | Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene. | Genome Res | 1997 |
| 9143497 | BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21. | Genomics | 1997 |
| 9325053 | A high-resolution PAC and BAC map of the SCA2 region. | Genomics | 1997 |
| 8661061 | Chromosomal localization of murine and human oligodendrocyte-specific protein genes. | Genomics | 1996 |
| 8954791 | The gene organization, chromosome location, and expression of a 55-kDa matrix protein (PRELP) of human articular cartilage. | Genomics | 1996 |
| 8896555 | Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. | Nat Genet | 1996 |