Literature DB >> 4694513

Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniques.

D S Borgaonkar, L Ebenezer, C I Scott, H M Golomb, G F Bahr.   

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Year:  1973        PMID： 4694513     DOI： 10.1007/bf00273186

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


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  7 in total

1.  [A new technic of karyotyping].

Authors:  R Berger
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1971-12-20

2.  The quinacrine fluorescence method of Y-chromosome identification.

Authors:  D H Hollander; D S Borgaonkar
Journal:  Acta Cytol       Date:  1971 Sep-Oct       Impact factor: 2.319

3.  Quinacrine fluorescence of the human Y chromosome.

Authors:  D S Borgaonkar; D H Hollander
Journal:  Nature       Date:  1971-03-05       Impact factor: 49.962

4.  Identification of human chromosomes by DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson; E J Modest
Journal:  Chromosoma       Date:  1970       Impact factor: 4.316

5.  An infant with 45 chromosomes including a D-E (13-15-17-18) translocation chromosome.

Authors:  D S Borgaonkar; E Mules; C I Scott
Journal:  Johns Hopkins Med J       Date:  1971-05

6.  A balanced 13-18 translocation [46,XY,t(13q-;18q+)] in the father of an infant with multiple anomalies.

Authors:  E McGilvray; T Kajii; M Freund; F Bamatter; D Klein
Journal:  Humangenetik       Date:  1971

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
  7 in total
  6 in total

1.  18Q - syndrome resulting from a tdic(14p; 18q).

Authors:  J C Lambert; M Ferrari; C Bergondi; A Galliana; N Ayraud
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

2.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975

Review 3.  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

4.  Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.

Authors:  D P Duckett; S H Roberts; P Davies
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  The use of agarose in the determination of anchorage-independent growth.

Authors:  A I Neugut; I B Weinstein
Journal:  In Vitro       Date:  1979-05

Review 6.  Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.

Authors:  D P Duckett; S H Roberts
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  6 in total

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