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PMID: 4140836 Published · ppublish English Journal Article

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

Humangenetik ·Vol. 24 ·No. 3 ·1974-00-00 ·Pages 247-52

Fryns JP, Van Den Berghe H

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Chromosome Aberrations Chromosomes, Human, 6-12 and X Heart Defects, Congenital/genetics Humans Infant, Newborn Karyotyping Male Pedigree Staining and Labeling Translocation, Genetic Trisomy
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fryns J P
Van Den Berghe H
References (26)
26 references, click to expand
  1. A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).
    J Med Genet. 1970 Mar;7(1):77-80 PMID: 5480968
  2. [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].
    Arch Fr Pediatr. 1967 Oct;24(8):859-68 PMID: 5584189
  3. MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.
    Cytogenetics. 1965;4:45-64 PMID: 14291491
  4. A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.
    Arch Dis Child. 1969 Feb;44(233):106-12 PMID: 5765976
  5. Two familial translocations involving the 6-12 group. With meiotic studies in one.
    Teratology. 1968 May;1(2):135-51 PMID: 5759133
  6. New translocation in three generations of a family.
    J Med Genet. 1968 Sep;5(3):200-4 PMID: 5708024
  7. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Ann Genet. 1970 Dec;13(4):217-32 PMID: 5313386
  8. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Ann Genet. 1968 Sep;11(3):171-5 PMID: 5304617
  9. [Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].
    Z Kinderheilkd. 1971;109(4):293-9 PMID: 5555168
  10. Partial trisomy of chromosome 11: a case report.
    Am J Ment Defic. 1973 Jan;77(4):383-8 PMID: 4706396
  11. Identification of partial 12 trisomy by quinacrine fluorescence.
    J Pediatr. 1973 Feb;82(2):269-72 PMID: 4119313
  12. [6-12 13-15 translocation and partial 6-12 trisomy (probably 10)].
    Ann Genet. 1965;8(1):16-20 PMID: 5294576
  13. Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
    Humangenetik. 1971;12(3):175-81 PMID: 5563410
  14. [Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].
    Ann Genet. 1969 Jun;12(2):133-7 PMID: 5308386
  15. [2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].
    Ann Genet. 1972 Jun;15(2):85-92 PMID: 4537727
  16. Familial reciprocal C/18 translocation.
    Am J Hum Genet. 1966 Nov;18(6):572-83 PMID: 5927877
  17. A case of tertiary trisomy due to C-C translocation in the mother.
    Jinrui Idengaku Zasshi. 1972 Sep;17(1):44-9 PMID: 4676027
  18. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Humangenetik. 1973 Apr 16;18(2):129-38 PMID: 4124236
  19. MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME.
    Lancet. 1964 Oct 17;2(7364):838-40 PMID: 14197160
  20. [Cp trisomy: a new syndrome].
    Ann Genet. 1971 Sep;14(3):177-86 PMID: 5315464
  21. [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].
    Humangenetik. 1973;18(4):321-7 PMID: 4200006
  22. [Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].
    Ann Genet. 1966;9(1):12-8 PMID: 5295698
  23. [Primary testicular hypotrophy. Karyotype XY with 12-10 translocation].
    Ann Endocrinol (Paris). 1966 Mar-Apr;27(2):155-60 PMID: 5944437
  24. [Partial C trisomy through translocation t(Cp-;Gp-)].
    Ann Genet. 1969 Mar;12(1):36-45 PMID: 5306710
  25. [Multiple malformations in partial trisomy C (12) as manifestation of an inherited E-C (18/12) translocation].
    Helv Paediatr Acta. 1967 Apr;22(1):41-53 PMID: 5585048
  26. 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.
    Ann Genet. 1969 Mar;12(1):15-27 PMID: 5306708
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
Published
1974-00-00
Pages
247-52
Language
English
Region
Germany
NLM ID
7607154
Subset
IM
External Links
PubMed source
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