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Volumn 55, Issue 3, 2000, Pages 335-340

A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN DEVELOPMENT; CHILD; CHROMOSOME 3P; CHROMOSOME MAP; CLINICAL ARTICLE; DISABILITY; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; MALE; MENTAL DEFICIENCY; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

EID: 0033837814     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.3.335     Document Type: Article
Times cited : (49)

References (44)
  • 1
    • 85037923635 scopus 로고
    • Disability in America: Toward a national agenda for prevention. Washington, DC: National Academy Press
    • (1991)
    • Pope, A.M.1    Tarlov, A.R.2
  • 2
    • 0008176324 scopus 로고    scopus 로고
    • Children with disabilities. Baltimore: Paul H. Brookes Publishing Co.
    • (1997)
    • Batshaw, M.1
  • 6
    • 0002716351 scopus 로고
    • Developmental delays
    • Hoekelman RA, Friedman SB, Nelson NM, Seidel HM, eds. Primary pediatric care. 2nd ed. St. Louis: Mosby Year-Book
    • (1992) , pp. 867-870
    • Simeonsson, R.J.1    Sharp, M.C.2
  • 9
    • 0018121860 scopus 로고
    • Mental retardation and multiple congenital anomalies of unknown etiology: Frequency of occurrence in similarly affected sibs of the proband
    • (1978) Birth Defects , vol.14 , pp. 127-137
    • Bartley, J.A.1    Hall, B.D.2
  • 15
    • 0032901062 scopus 로고    scopus 로고
    • Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres
    • (1999) J Med Genet , vol.36 , pp. 405-411
    • Slavotinek, A.1    Rosenberg, M.2    Knight, S.3
  • 21
  • 22
    • 16044371402 scopus 로고    scopus 로고
    • National Institutes of Health and Institute of Molecular Medicine collaboration. A complete set of human telomeric probes and their clinical application
    • (1996) Nat Genet , vol.14 , pp. 86-89
  • 26
    • 0025166530 scopus 로고
    • Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: Karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3
    • (1990) Am J Hum Genet , vol.35 , pp. 269-273
    • Narahara, K.1    Kikkawa, K.2    Murakami, M.3
  • 28
  • 31
    • 0008281457 scopus 로고
    • Smith's recognizable patterns of human malformations. Philadelphia: WB Saunders
    • (1988)
    • Jones, K.L.1
  • 40
    • 0032965439 scopus 로고    scopus 로고
    • Localization of the human caveolin-3 gene to the D3S18/D3S4163/D3S4539 locus (3p25), in close proximity to the human oxytocin receptor gene. Identification of the caveolin-3 gene as a candidate for deletion in 3p- syndrome
    • (1999) FEBS Lett , vol.452 , pp. 177-180
    • Sotgia, F.1    Minetti, C.2    Lisanti, M.P.3
  • 42
    • 0027096397 scopus 로고
    • Regulation of axonal growth in the vertebrate nervous system by interactions between glycoproteins belonging to two subgroups of the immunoglobulin superfamily
    • (1992) J Cell Biol , vol.119 , pp. 1387-1394
    • Sonderegger, P.1    Rathjen, F.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.