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J-GLOBAL ID:201602220670436400   Reference number:16A0041373

A Girl with Partial Monosomy 3p/Partial Trisomy 3q

3番染色体短腕端部部分モノソミー/3番染色体長腕端部部分トリソミーを合併した一女児例
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Material:
Volume: 51  Issue:Page: 1260-1264  Publication year: Dec. 10, 2015 
JST Material Number: Z0500B  ISSN: 1348-964X  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Diagnostics of congenital diseases, deformities.  ,  Mental disorders  ,  Gynecologic and obstetric diagnosis 
Reference (24):
  • Steinbach P, Adkins WN Jr, Caspar H et al. : The dup (3q) syndrome : report of eight cases and review of the literature. Am J Med Genet 1981 ; 10 : 159-177
  • Kline AD, Barr M, Jackson LG, et al. : Growth manifestations in the Brachmann-de Lange syndrome. Am J Med Genet 1993 ; 47 : 1042-9
  • Allderdice PW, Browne N, Murphy DP : Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv (3) (p25q21). Am J Hum Genet 1975 ; 27 : 699-718
  • Falek A, Schmidt R, Jervis GA : Familial de Lange syndrome with chromosome abnormalities. Pediatrics 1966 ; 37 : 92-101
  • Fernandez Alvarez JR, Amess PN, Gandhi RS, et al. : Diagnostic value of subependymal pseudocysts and choroid plexus cysts on neonatal cerebral ultrasound : a meta-analysis. Arch Dis Child Fetal Neonatal Ed 2009 ; 94 : F443-6
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