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Pregled bibliografske jedinice broj: 191943

Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I


Petković, Iskra; de Capoa, Adriana; Giancotti, Paola; Barišić, Ingeborg
Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I // Clinical Genetics, 50 (1996), 6; 515-519 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 191943 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I
(Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.)

Autori
Petković, Iskra ; de Capoa, Adriana ; Giancotti, Paola ; Barišić, Ingeborg

Izvornik
Clinical Genetics (0009-9163) 50 (1996), 6; 515-519

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
chromosome polymorphism; chromosome segregation; rare unbalanced t(11; 22); t(11; 22)

Sažetak
Reciprocal translocation t(11 ; 22)(q23 ; q11) is of particular interest because the unbalanced offspring of the translocation carriers usually present with a supernumerary derivative chromosome 22. This common unbalanced karyotype is the result of 3:1 chromosome segregation during meiosis. We report the third case of a rare segregation pattern of a paternal 11 ; 22 translocation. The proband's karyotype revealed the presence of a der(11) and two copies of a der(22), i.e. 47, XX, t(11 ; 22)(q23 ; q11), +der(22) t(11 ; 22)pat. The karyotype is the result of paternal 3:1 segregation after crossing-over involving the derived and the normal chromosome 22, as revealed by chromosome polymorphism analysis. Contrary to the preferential maternal, transmission of this common unbalanced translocation, the data from the literature, including our case, may suggest preferential paternal transmission of this rare type of unbalanced translocation.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta

Profili:

Avatar Url Ingeborg Barišić (autor)

Avatar Url Iskra Petković (autor)


Citiraj ovu publikaciju:

Petković, Iskra; de Capoa, Adriana; Giancotti, Paola; Barišić, Ingeborg
Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I // Clinical Genetics, 50 (1996), 6; 515-519 (međunarodna recenzija, članak, znanstveni)
Petković, I., de Capoa, A., Giancotti, P. & Barišić, I. (1996) Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I. Clinical Genetics, 50 (6), 515-519.
@article{article, author = {Petkovi\'{c}, Iskra and de Capoa, Adriana and Giancotti, Paola and Bari\v{s}i\'{c}, Ingeborg}, year = {1996}, pages = {515-519}, keywords = {chromosome polymorphism, chromosome segregation, rare unbalanced t(11, 22), t(11, 22)}, journal = {Clinical Genetics}, volume = {50}, number = {6}, issn = {0009-9163}, title = {Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I}, keyword = {chromosome polymorphism, chromosome segregation, rare unbalanced t(11, 22), t(11, 22)} }
@article{article, author = {Petkovi\'{c}, Iskra and de Capoa, Adriana and Giancotti, Paola and Bari\v{s}i\'{c}, Ingeborg}, year = {1996}, pages = {515-519}, keywords = {chromosome polymorphism, chromosome segregation, rare unbalanced t(11, 22), t(11, 22)}, journal = {Clinical Genetics}, volume = {50}, number = {6}, issn = {0009-9163}, title = {Unusual segregation of t(11 ; 22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.}, keyword = {chromosome polymorphism, chromosome segregation, rare unbalanced t(11, 22), t(11, 22)} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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