Literature DB >> 4139262

Inherited partial duplication of chromosome No. 15.

A Fujimoto, J W Towner, A J Ebbin, E J Kahlstrom, M G Wilson.   

Abstract

Mesh：

Year:  1974        PMID： 4139262      PMCID： PMC1013145          DOI： 10.1136/jmg.11.3.287

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


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  6 in total

1.  Partial trisomy of chromosome 15.

Authors:  W Bucher; C E Parker; B Crandall; O S Alfi
Journal:  Lancet       Date:  1973-06-02       Impact factor: 79.321

2.  Partial trisomy of chromosome 15.

Authors:  C E Parker; O S Alfi
Journal:  Lancet       Date:  1972-05-13       Impact factor: 79.321

3.  Partial trisomy 15.

Authors:  R E Magenis; K M Overton; J A Reiss; J P Macfarlane; F Hecht
Journal:  Lancet       Date:  1972-12-23       Impact factor: 79.321

4.  Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding.

Authors:  B F Crandall; H M Muller; H N Bass
Journal:  Am J Ment Defic       Date:  1973-03

5.  Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.

Authors:  M M Cohen; V J Capraro; N Takagi
Journal:  Ann Hum Genet       Date:  1967-05       Impact factor: 1.670

6.  Pericentric inversion of a number 15 chromosome in nine members of one family.

Authors:  B F Crandall; R S Sparkes
Journal:  Cytogenetics       Date:  1970
  6 in total
  20 in total

1.  Partial trisomy D: a diagnostic and cytogenetic dilemma.

Authors:  M M Cohen; A Rosenmann; J Dagan; C Legum
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

2.  Nonrandom distribution of exchange points in patients with structural rearrangements.

Authors:  Y Nakagome; H Chiyo
Journal:  Am J Hum Genet       Date:  1976-01       Impact factor: 11.025

3.  Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

Authors:  D Wieczorek; H Engels; R Viersbach; B Henke; G Schwanitz; E Passarge
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

4.  A case of de novo duplication of 15q24-q26.3.

Authors:  Eun Young Kim; Yu Kyong Kim; Mi Kyoung Kim; Ji Mi Jung; Ga Won Jeon; Hye Ran Kim; Jong Beom Sin
Journal:  Korean J Pediatr       Date:  2011-06-30

5.  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

6.  Distal 15q trisomy: phenotypic comparison of nine cases in an extended family.

Authors:  P Schnatterly; K L Bono; M Robinow; H E Wyandt; N Kardon; T E Kelly
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

7.  A complex chromosome rearrangement resulting in trisomy 15q22 to qter.

Authors:  P N Howard-Peebles; P R Scarbrough; J Sharpe; W H Finley; S C Finley
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318

Review 8.  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

9.  Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

Authors:  E Blennow; H Telenius; D de Vos; C Larsson; P Henriksson; O Johansson; N P Carter; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

10.  Two familial cases with trisomy 15q dist due to a rcp(5;15)(p14;q21).

Authors:  M Tzancheva; M Krachounova; Z Damjanova
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
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