Literature DB >> 4142590

The supernumerary isochromosome 18 syndrome (+ 18pu).

C J Condron, R J Cantwell, R L Kaufman, S B Brown, R J Warren.   

Abstract

Mesh：

Year:  1974        PMID： 4142590

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  6 in total

1.  Extra small metacentric chromosome identified as i(18p).

Authors:  M Rocchi; M Stormi; N Archidiacono; G Filippi
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

2.  Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.

Authors:  R Plattner; N A Heerema; P N Howard-Peebles; J H Miles; S Soukup; C G Palmer
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

3.  Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

Authors:  L M Larson; W A Wasdahl; J H Saumur; M L Coleman; S M Jalal
Journal:  J Med Genet       Date:  1978-02       Impact factor: 6.318

4.  Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes.

Authors:  R Plattner; N A Heerema; Y B Yurov; C G Palmer
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

5.  Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome.

Authors:  K B Nielsen; H Dyggve; U Friedrich; N Hobolth; T Lyngbye; M Mikkelsen
Journal:  Hum Genet       Date:  1978-10-19       Impact factor: 4.132

6.  Tetrasomy 18p: case report and review of literature.

Authors:  Shahad Bawazeer; Maha Alshalan; Aziza Alkhaldi; Nasser AlAtwi; Mohammed AlBalwi; Abdulrahman Alswaid; Majid Alfadhel
Journal:  Appl Clin Genet       Date:  2018-02-08
  6 in total

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