Literature DB >> 7390479

A new R-banding technique in clinical cytogenetics.

G S Pai, G H Thomas.   

Abstract

Currently, standard methods of chromosome banding detect an abnormality in some 10%--15% of all patients referred for a cytogenetic study. Higher resolution by the study of the less contracted chromosomes with or without cell synchronization techniques may yield higher frequencies in the future. On the other hand, use of more complicated methodology adds to the time and expense needed for the study. The method of 5' bromodeoxyuridine pretreatment of cells in culture is commonly used to study the replication behavior of X chromosomes, and is known to demonstrate R bands along the other chromosomes. We have modified this technique with the addition of a cell synchronization step and evaluated several variables that are of importance in a clinical service laboratory setting. The method offers a simple way to obtain quality R-banded karyotypes. The advantages and limitations, based on our study of 120 consecutive cultures, are described.

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Year:  1980        PMID: 7390479     DOI: 10.1007/bf00279047

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


  11 in total

1.  High resolution of human chromosomes.

Authors:  J J Yunis
Journal:  Science       Date:  1976-03-26       Impact factor: 47.728

2.  [Descriptive diagrams of human chromosomes (R band analysis and nomenclature according to the conference in Paris in 1971)].

Authors:  M Prieur; B Dutrillaux; J Lejeune
Journal:  Ann Genet       Date:  1973-03

3.  A simple technique for demonstrating centromeric heterochromatin.

Authors:  A T Sumner
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

4.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321

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.  An extra band in human 9qh+ chromosomes.

Authors:  K Madan
Journal:  Hum Genet       Date:  1978-09-19       Impact factor: 4.132

7.  The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.

Authors:  T Caspersson; G Lomakka; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

8.  Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes.

Authors:  U Francke; N Oliver
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

9.  A simple R banding technic.

Authors:  R S Verma; H A Lubs
Journal:  Am J Hum Genet       Date:  1975-01       Impact factor: 11.025

10.  [Discontinued treatment with BudR and staining with acridine orange: observation of R- or Q- or intermediary banding (author's transl)].

Authors:  B Dutrillaux
Journal:  Chromosoma       Date:  1975-10-14       Impact factor: 4.316

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  18 in total

1.  Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?

Authors:  K R Held; S Kerber; E Kaminsky; S Singh; P Goetz; E Seemanova; H W Goedde
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

2.  High-resolution dynamic and morphological G-bandings (GBG and GTG): a comparative study.

Authors:  N Lemieux; R Drouin; C L Richer
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

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.  Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

Authors:  C E Schwartz; J P Johnson; B Holycross; T M Mandeville; T S Sears; E A Graul; J C Carey; R J Schroer; M C Phelan; J Szollar
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

5.  High resolution R banding in amniotic fluid cells using the BrdU-Hoechst 33258-Giemsa (RBG) technique.

Authors:  S W Cheung; J P Crane; A C Burgess
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  Localization of the spherocytosis gene to chromosome segment 8p11.22----8p21.

Authors:  M Kitatani; H Chiyo; M Ozaki; S Shike; S Miwa
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

7.  The parental origin and mechanism of formation of three dicentric X chromosomes.

Authors:  M C Phelan; L A Prouty; R E Stevenson; P N Howard-Peebles; D C Page; C E Schwartz
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

8.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

9.  Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

Authors:  M C Phelan; C C Morton; R E Stevenson; R E Tanzi; G D Stewart; P C Watkins; J F Gusella; J A Amos
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

10.  SRVX, a sex reversing locus in Xp21.2-->p22.11.

Authors:  P Arn; H Chen; C M Tuck-Muller; C Mankinen; G Wachtel; S Li; C C Shen; S S Wachtel
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

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