Literature DB >> 8558566

Duplication 2 (q11.2-q21): a previously unreported abnormality.

L B Cooke1, H Richards, P W Lunt, L Burvill-Holmes, R T Howell, A McDermott.   

Abstract

Mesh：

Year:  1995        PMID： 8558566      PMCID： PMC1051712          DOI： 10.1136/jmg.32.10.825

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

1.  Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.

Authors:  M Zankl; G Schwanitz; P Schmid; H Zankl; G Dockter; A Rodewald; K D Zang; K P Grosse
Journal:  Am J Med Genet       Date:  1979

2.  Delineation of a characteristic phenotype in distal trisomy 2q.

Authors:  M Kyllerman; J Wahlström; B Westerberg; K H Gustavson
Journal:  Helv Paediatr Acta       Date:  1984-12
  2 in total
  1 in total

1.  The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes.

Authors:  Fang Xu; Ya-Nan Zhang; De-Hua Cheng; Ke Tan; Chang-Gao Zhong; Guang-Xiu Lu; Ge Lin; Yue-Qiu Tan
Journal:  Mol Cytogenet       Date:  2014-10-03       Impact factor: 2.009
  1 in total

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