Literature DB >> 5114675

Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.

P W Allderdice, O J Miller, D A Miller, W R Breg, E Gendel, C Zelson.   

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Year:  1971        PMID： 5114675     DOI： 10.1007/bf00326943

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


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  5 in total

1.  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

2.  A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome.

Authors:  J R Miller; F J Dill; M J Corey; J M Rigg
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318

3.  A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.

Authors:  F Nuzzo; A Marini; C Baglioni; C E Ford; L De Carli; L Piceni Sereni
Journal:  Cytogenetics       Date:  1968

4.  A complex familial translocation involving chromosomes 5, 9 and 13.

Authors:  K Fredga; B Hall
Journal:  Cytogenetics       Date:  1970

5.  Presumptive C-15 translocation and familial large Y identified by autoradiography.

Authors:  A De Capoa; F H Allen; A P Gold; R Koenigsberger; O J Miller
Journal:  J Med Genet       Date:  1969-03       Impact factor: 6.318
  5 in total
  30 in total

1.  Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.

Authors:  C G Palmer; C Poland; T Reed; J Kojetin
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

2.  The syndrome of partial trisomy 14q.

Authors:  F Lo Curto; P Maraschio; P Milanesi; F Severi; A C Ugazio; O Zuffardi
Journal:  Eur J Pediatr       Date:  1976-11-03       Impact factor: 3.183

3.  Partial trisomy 14q due to familial t(14q-,11q+) translocation.

Authors:  J P Fryns; M Van Eygen; W Tanghe; H Van Den Berghe
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

4.  46,XX/47XX, + 14 mosaicism in a liveborn infant.

Authors:  A O Martin; M M Ford; N T Khalil; K B Turk; M N Macintyre
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

5.  Partial trisomy of the distal segment 14q.

Authors:  Y Nakamura; K Sakai; S Sakuma; E Sato; M Maruyama; T Hashimoto; S Fukuda; Y Nishimi; Y Nakagome; Y Nakahori
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

6.  Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Authors:  M H Bogart; C L Bradshaw; O W Jones; J E Schanberger
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

7.  Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22).

Authors:  G Kovacs; C Mihai
Journal:  Hum Genet       Date:  1979-06-19       Impact factor: 4.132

8.  Familial partial 14 trisomy.

Authors:  J Q Miller; K Willson; H Wyandt; M A Jaramillo; T S McConnell
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

9.  Tertiary trisomy, 47,XX,+14q--, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24).

Authors:  S R Young; D M Donovan; H A Greer; K Burch; D C Potter
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132

10.  Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.

Authors:  J B Bijlsma; H F de France; L M Bleeker-Wagemakers; P F Dijkstra
Journal:  Hum Genet       Date:  1978-01-19       Impact factor: 4.132
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