Literature DB >> 5046909

Quinacrine fluorescence patterns in somatic chromosomes of a t(15q15q) carrier.

M C Yoshida, N Nomoto, M Sasaki.   

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Year:  1972        PMID： 5046909     DOI： 10.1007/bf00273432

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  13 in total

1.  Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations.

Authors:  F Hecht; M P Case; E W Lovrien; J V Higgins; H C Thuline; J Melnyk
Journal:  Science       Date:  1968-07-26       Impact factor: 47.728

2.  Difference in fluorescence of the homologe chromosomes No. 3 in man.

Authors:  W Schnedl
Journal:  Humangenetik       Date:  1971

3.  Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence.

Authors:  M L O'Riordan; J A Robinson; K E Buckton; H J Evans
Journal:  Nature       Date:  1971-03-19       Impact factor: 49.962

4.  Quinacrine fluorescence patterns of human D group chromosomes.

Authors:  D A Miller; P W Allderdice; O J Miller; W R Breg
Journal:  Nature       Date:  1971-07-02       Impact factor: 49.962

5.  DNA replication studies of human D-group chromosomes in satellite associations.

Authors:  Y Nakagome
Journal:  Cytogenetics       Date:  1969

6.  Non-random association of human acrocentric chromosomes.

Authors:  S R Patil; H A Lubs
Journal:  Humangenetik       Date:  1971

7.  The inheritance of translocations in man: data from families ascertained through a balanced heterozygote.

Authors:  P A Jacobs; J Aitken; A Frackiewicz; P Law; M S Newton; P G Smith
Journal:  Ann Hum Genet       Date:  1970-10       Impact factor: 1.670

8.  Random association of human acrocentric chromosomes.

Authors:  M W Shaw; A P Craig; F C Ricciuti
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

9.  Translocation between both members of chromosome pair number 15 causing recurrent abortions.

Authors:  M Lucas
Journal:  Ann Hum Genet       Date:  1969-05       Impact factor: 1.670

10.  Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.

Authors:  T Caspersson; M Hultén; J Lindsten; A J Therkelsen; L Zech
Journal:  Hereditas       Date:  1971       Impact factor: 3.271
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  5 in total

1.  Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions.

Authors:  L M Farah; H R de Nazareth; M Dolnikoff; D Delascio
Journal:  Humangenetik       Date:  1975-08-25

2.  Translocation D/D involving two homologous chromosomes of the pair 15.

Authors:  J Zizka; P Balícek; A Finková
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

3.  Giemsa banding in the t(13q13q) carrier mother of a translocation trisomy 13 abortus.

Authors:  M I Parslow; R J Gardner; A M Veale
Journal:  Humangenetik       Date:  1973-04-16

4.  15/15 translocation in Prader-Willi syndrome.

Authors:  M Fraccaro; O Zuffardi; E M Buhler; L P Jurik
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

5.  Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Authors:  M Fraccaro; O Zuffardi; E Bühler; A Schinzel; G Simoni; R Witkowski; E Bonifaci; D Caufin; G Cignacco; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  5 in total

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