Literature DB >> 511166

A new case of partial trisomy 15q-.

A Geneix, J Y Jaffray, P Malet, E Foulon, P Jalbert, P Crost.   

Abstract

Partial trisomy 15 was observed in a newborn with malformations of the head and extremities. A t(5;15) translocation was found in the mother and maternal grandfather.

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Mesh：

Year:  1979        PMID： 511166     DOI： 10.1007/bf00283405

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  6 in total

1.  An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.

Authors:  M M Cohen; A Ornoy; A Rosenmann; G Kohn
Journal:  Ann Genet       Date:  1975-06

2.  A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange.

Authors:  D L Bannister; E Engel
Journal:  J Pediatr       Date:  1975-06       Impact factor: 4.406

3.  Familial partial trisomy 15.

Authors:  M M Power; R G Barry; D E Cannon; J G Masterson
Journal:  Ann Genet       Date:  1977-09

4.  A case of partial trisomy 15.

Authors:  E J Watson; R R Gordon
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

5.  [A new technic of analysis of the human karyotype].

Authors:  B Dutrillaux; J Lejeune
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1971-05-17

6.  Human gene mapping using an X/autosome translocation.

Authors:  E Solomon; M Bobrow; P N Goodfellow; W F Bodmer; D M Swallow; S Povey; B Noël
Journal:  Somatic Cell Genet       Date:  1976-03
  6 in total
  4 in total

1.  Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter).

Authors:  D J Goldstein; R E Ward; W C Nichols; C G Palmer
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

2.  De novo partial trisomy 15q (proximal type).

Authors:  T J Herweijer; J W Oorthuys; N J Leschot
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

Review 3.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

Authors:  A Schinzel; W Schmid; M Fraccaro; L Tiepolo; O Zuffardi; J M Opitz; J Lindsten; P Zetterqvist; H Enell; C Baccichetti; R Tenconi; R A Pagon
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  4 in total

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