Literature DB >> 3874588

De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.

J P Fryns, M Haspeslagh, A Agneessens, H van den Berghe.   

Abstract

In the present paper a malformed male newborn is presented with de novo 2q3 trisomy/distal 7p22 monosomy and typical clinical findings of 7p deletion syndrome including trigonocephaly.

Entities:  

Mesh：

Year:  1985        PMID： 3874588

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  4 in total

Review 1.  Genetic markers on chromosome 7.

Authors:  L C Tsui
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

2.  Chromosome 7 short arm deletion, 7p21----pter.

Authors:  M Schömig-Spingler; M Schmid; W Brosi; T Grimm
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

Review 3.  De novo terminal deletion 7p22.1--pter in a child without craniosynostosis.

Authors:  F Speleman; M Craen; J Leroy
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

4.  Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.

Authors:  J P Fryns; A Kleczkowska; E Kubień; H Van den Berghe
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132
  4 in total

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