Literature DB >> 4737101

A familial translocation t(6q+;8q-) identified by fluorescence microscopy.

E Niebuhr.   

Abstract

Mesh：

Year:  1973        PMID： 4737101     DOI： 10.1007/bf00291490

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


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  10 in total

1.  Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.

Authors:  T Caspersson; J Lindsten; L Zech; K E Buckton; W H Price
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

2.  Prenatal diagnosis of chromosome abnormalities.

Authors:  A J Therkelsen; G B Petersen; O R Steenstrup; J Jonasson; J Lindsten; L Zech
Journal:  Acta Paediatr Scand       Date:  1972-07

3.  C8 trisomy mosaicism syndrome.

Authors:  J B Bijlsma; J C Wijffels; W H Tegelaers
Journal:  Helv Paediatr Acta       Date:  1972-07

4.  Two human X-autosome translocations identified by autoradiography and fluorescence.

Authors:  M M Cohen; C C Lin; V Sybert; E J Orecchio
Journal:  Am J Hum Genet       Date:  1972-09       Impact factor: 11.025

5.  [Translocation 8-22 with no length change and partial trisomy for 8q. Detection by heat denaturation].

Authors:  J Lejeune; M O Rethore; B Dutrillaux; G Martin
Journal:  Exp Cell Res       Date:  1972-09       Impact factor: 3.905

6.  [Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].

Authors:  J de Grouchy; C Turleau; C Léonard
Journal:  Ann Genet       Date:  1971-03

7.  Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.

Authors:  L J Butler; S M Eades; N E France
Journal:  Ann Genet       Date:  1969-03

8.  [A further case of presumed 6-12 trisomy].

Authors:  P Jalbert; J Jobert; J Patet; C Mouriquand; J Roget
Journal:  Ann Genet       Date:  1966-09

9.  Trisomy C in an infant with polycystic kidneys and other malformations.

Authors:  R C Juberg; E F Gilbert; R S Salisbury
Journal:  J Pediatr       Date:  1970-04       Impact factor: 4.406

10.  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
  10 in total
  2 in total

1.  New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome.

Authors:  A Rodewald; S Stengel-Rutkowski; P Schulz; H Cleve
Journal:  Eur J Pediatr       Date:  1977-04-26       Impact factor: 3.183

2.  Brother and sister with trisomy 10p: a new syndrome.

Authors:  E Schleiermacher; U Schliebitz; C Steffens
Journal:  Humangenetik       Date:  1974
  2 in total

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