Literature DB >> 6831761

High resolution chromosome banding in the Rubinstein-Taybi syndrome.

E A Wulfsberg, I J Klisak, R S Sparkes.   

Abstract

We studied eight cases of the Rubinstein-Taybi syndrome to determine if a detectable chromosome change is associated with this syndrome. High resolution G-banded analysis of prometaphase chromosomes was carried out on venous blood with two to four karyotypes analyzed for each patient. Initial study of two patients suggested an abnormality in chromosome 15q, but blinded analysis and review of the karyotypes proved to be normal. Therefore, all eight patients had normal G-banded prometaphase chromosome studies. Because of technical difficulties and observer bias, we urge caution in using high resolution chromosome studies to screen whole karyotypes for suspected abnormalities.

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Year:  1983        PMID: 6831761     DOI: 10.1111/j.1399-0004.1983.tb00434.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

1.  High resolution cytogenetic evaluation of couples with recurring fetal wastage.

Authors:  T L Yang-Feng; S C Finley; W H Finley; U Francke
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 2.  Rubinstein-Taybi syndrome.

Authors:  A C Berry
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

3.  Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

Authors:  V R Babu; D L Van Dyke; C E Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

4.  Chromosome 15 in Prader-Willi syndrome.

Authors:  C N Fear; D E Mutton; A C Berry; J Z Heckmatt; V Dubowitz
Journal:  Dev Med Child Neurol       Date:  1985-06       Impact factor: 5.449

  4 in total

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