Literature DB >> 1176148

Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.

H Schröchsnadel, C Feichtinger, C Scheminzky.   

Abstract

A trisomy 4p14 leads to 4pter in a 15-year-old girl is reported. The main features are physical and mental retardation and the absence of gross malformations. The relevance of other symptoms found in the patient is discussed.

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Year:  1975        PMID： 1176148     DOI： 10.1007/bf00394195

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


  19 in total

1.  A case of trisomy of the short arms of chromosome no. 4 with translocation t(4p 21p; 4q 21q) in the mother.

Authors:  M Furbetta; G Rosi; P Cossu; A Cao
Journal:  Humangenetik       Date:  1975

2.  [Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].

Authors:  B Dallapiccola; L Capra; G Preto; M Covic; B Dutrillaux
Journal:  Ann Genet       Date:  1974-06

3.  [Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)].

Authors:  M O Rethoré; B Dutrillaux; J C Job; J Lejeune
Journal:  Ann Genet       Date:  1974-06

4.  [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].

Authors:  G Giovannelli; A Forabosco; B Dutrillaux
Journal:  Ann Genet       Date:  1974-06

5.  Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

Authors:  L Owen; B Martin; C E Blank; F Harris
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

6.  [Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].

Authors:  F Metz; L Bier; R A Pfeiffer
Journal:  Humangenetik       Date:  1973-05-25

7.  Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.

Authors:  W L Gouw; G J Anders; L P ten Kate; C J de Groot
Journal:  Humangenetik       Date:  1972

8.  [Segregation of a balanced translocation t(5p-;Gp+)].

Authors:  B Noel; B Quack; M Thiriet
Journal:  Ann Genet       Date:  1968-12

9.  Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

Authors:  A De Capoa; D Warburton; W R Breg; D A Miller; O J Miller
Journal:  Am J Hum Genet       Date:  1967-07       Impact factor: 11.025

10.  [Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].

Authors:  C Laurent; J M Robert
Journal:  Ann Genet       Date:  1966-09
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  4 in total

1.  Hand dermatoglyphics in trisomy 4p.

Authors:  P Mastroiacovo; V Currò; A Calabro; B Dallapiccola
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

2.  Trisomy 4p due to a paternal t(4p-;16p+) translocation.

Authors:  T Bauknecht; F Betteken; W Vogel
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

3.  Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family.

Authors:  M Andrle; A Erlach; W Killian; A Rett
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

Review 4.  Clinical manifestations of trisomy 4p syndrome.

Authors:  S V Patel; H Dagnew; A J Parekh; E Koenig; R A Conte; M J Macera; R S Verma
Journal:  Eur J Pediatr       Date:  1995-06       Impact factor: 3.183
  4 in total

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