Literature DB >> 6974535

Pierre-Robin anomalad, moderate mental retardation and distal 4q deletion.

J P Fryns, J Timmermans, J Hoedemaekers, L Emmery, H Van den Berghe.   

Abstract

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Year:  1981        PMID： 6974535

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


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  4 in total

1.  A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.

Authors:  R D Jefferson; J Burn; K L Gaunt; S Hunter; E V Davison
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

2.  Del(4)(q33----qter): another case report of a child with mild dysmorphism.

Authors:  K A Fagan; R B Morris
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

3.  Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.

Authors:  J R Korenberg; H Kawashima; S M Pulst; T Ikeuchi; N Ogasawara; K Yamamoto; S A Schonberg; R West; L Allen; E Magenis
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

Review 4.  Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.

Authors:  Michael R Rossi; Miriam S DiMaio; Bixia Xiang; Kangmo Lu; Hande Kaymakcalan; Margretta Seashore; Maurice J Mahoney; Peining Li
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802
  4 in total

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