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Volumn 49, Issue 8, 2004, Pages 440-444

A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome

Author keywords

9q34.3 terminal deletion syndrome; Critical region; FISH

Indexed keywords

ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; GENETIC DISORDER; HUMAN; MALE; MOLECULAR CLONING; PHENOTYPE; TERMINAL DELETION SYNDROME;

EID: 4544241694     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-004-0166-z     Document Type: Article
Times cited : (37)

References (17)
  • 1
    • 0037189923 scopus 로고    scopus 로고
    • MIZIP, a highly conserved, vertebrate specific melanin-concentrating hormone receptor 1 interacting zinc-finger protein
    • Bachner D, Kreienkamp HJ, Richter D (2002) MIZIP, a highly conserved, vertebrate specific melanin-concentrating hormone receptor 1 interacting zinc-finger protein. FEBS Lett 28:124-128
    • (2002) FEBS Lett , vol.28 , pp. 124-128
    • Bachner, D.1    Kreienkamp, H.J.2    Richter, D.3
  • 5
    • 0038392953 scopus 로고    scopus 로고
    • The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation
    • Flint J, Knight S (2003) The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation. Curr Opin Genet Dev 13:310-316
    • (2003) Curr Opin Genet Dev , vol.13 , pp. 310-316
    • Flint, J.1    Knight, S.2
  • 11
    • 0034661199 scopus 로고    scopus 로고
    • Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone-releasing hormone (LHRH) neurons
    • Kramer PR, Wray S (2000) Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone-releasing hormone (LHRH) neurons. Genes Dev 14:1824-1834
    • (2000) Genes Dev , vol.14 , pp. 1824-1834
    • Kramer, P.R.1    Wray, S.2
  • 12
    • 0029162269 scopus 로고
    • Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
    • Ledbetter DH, Engel E (1995) Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum Mol Genet 4:1757-1764
    • (1995) Hum Mol Genet , vol.4 , pp. 1757-1764
    • Ledbetter, D.H.1    Engel, E.2
  • 14
    • 4544353657 scopus 로고    scopus 로고
    • A complex with chromatin modifiers that occupies E2F-and Myc-responsive genes in G0 cells
    • Ogawa H, Ishiguro K, Gaubatz S, Livingston DM, Nakatani Y (2002) A complex with chromatin modifiers that occupies E2F-and Myc-responsive genes in G0 cells. Science 10:1034-1035
    • (2002) Science , vol.10 , pp. 1034-1035
    • Ogawa, H.1    Ishiguro, K.2    Gaubatz, S.3    Livingston, D.M.4    Nakatani, Y.5
  • 15
    • 0033358738 scopus 로고    scopus 로고
    • Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity
    • Saar K, Al-Gazali L, Sztriha L, Rueschendorf F, Nur-E-Kamal M, Reis A, Bayoumi R (1999) Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity. Am J Hum Genet 65:1666-1671
    • (1999) Am J Hum Genet , vol.65 , pp. 1666-1671
    • Saar, K.1    Al-Gazali, L.2    Sztriha, L.3    Rueschendorf, F.4    Nur-E-Kamal, M.5    Reis, A.6    Bayoumi, R.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.