Literature DB >> 4119313

Identification of partial 12 trisomy by quinacrine fluorescence.

I A Uchida, C C Lin.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1973        PMID: 4119313     DOI: 10.1016/s0022-3476(73)80165-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  15 in total

1.  Syndrome +12p. Case report and review.

Authors:  R Tenconi; E Piovan; A Preto; R Magnabosco; C Baccichetti
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

2.  Two cases of trisomy 12p due to rcpt (12;21)(p11;p11) inherited through three generations.

Authors:  M Parslow; D Chambers; M Drummond; W Hunter
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

3.  Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.

Authors:  N Hobolth; P Jacobsen; M Mikkelsen
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

4.  Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.

Authors:  O Sanchez; J J Yunis; J I Escobar
Journal:  Humangenetik       Date:  1974-04-24

5.  A 21-21 tandem translocation with satellites on both long and short arms.

Authors:  B E Schuh; B R Korf; M J Salwen
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

6.  A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat.

Authors:  H Nielsen; M Vetner; V Holm; S Askjaer; E Reske-Nielsen
Journal:  Hum Genet       Date:  1977-03-14       Impact factor: 4.132

7.  Trisomy 12p due to familial t(12p-,6q plus) translocation.

Authors:  J P Fryns; H Van Den Berghe
Journal:  Humangenetik       Date:  1974

8.  Translocations involving chromosome 12. I. A report of a 12,21 translocation in a woman with recurrent abortions, and a study of the breakpoints and modes of ascertainment of translocations involving chromosome 12.

Authors:  J H Ford; R H Rofe; R P Pavy
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  New chromosomal dysmorphic syndromes. 4. Trisomy 12p.

Authors:  S Stengel-Rutkowski; A Albert; J D Murken; K Zahn-Messow; A Rodewald; M Zankl; H Saule; J Stene
Journal:  Eur J Pediatr       Date:  1981-07       Impact factor: 3.183

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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.