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Literature DB >> 631851

t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring.

N Archidiacono, M Rocchi, U de Vonderweid, G Filippi.

Abstract

A case of trisomy 9p originating from t(9/22) mat is reported. The rearrangement is characterized by centric fission of chromosome 9 and by translocation of NOR from chromosome 22 to 9q. The hypothesis of centric fission is discussed on the basis of various banding patterns. The case also reveals unusual knee dislocation.

Entities: Species

Mesh：

Year: 1978 PMID： 631851 DOI： 10.1007/bf00272193

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

22 in total

1. Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

Authors: C E Blank; D C Colver; A M Potter; J McHugh; J Lorber
Journal: Clin Genet Date: 1975-04 Impact factor: 4.438

2. Structure and inheritance of some heterozygous Robertsonian translocation in man.

Authors: A Daniel; P R Lam-Po-Tang
Journal: J Med Genet Date: 1976-10 Impact factor: 6.318

3. Dicentric X isochromosomes in man.

Authors: R T Howell; S H Roberts; R J Beard
Journal: J Med Genet Date: 1976-12 Impact factor: 6.318

4. Differential staining patterns of heterochromatin in man.

Authors: R Gagné; R Tanguay; C Laberge
Journal: Nat New Biol Date: 1971-07-07

5. A human family suggesting evidence for centric fission and stability of a telocentric chromosome.

Authors: A K Sinha; S Pathak; J J Nora
Journal: Hum Hered Date: 1972 Impact factor: 0.444

6. Fission in the evolution of a lizard karyotype.

Authors: T P Webster; W P Hall; E E Williams
Journal: Science Date: 1972-08-18 Impact factor: 47.728

7. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].

Authors: M O Rethoré; L Larget-Piet; D Abonyi; M Boeswillwald; R Berger; S Carpentier; J Cruveiller; B Dutrillau; J Lafourcade; M Penneau; J Lejeune
Journal: Ann Genet Date: 1970-12

8. Trisomy 9p syndrome and XYY syndrome in siblings.

Authors: K H Gustavson; J Wahlström
Journal: Clin Genet Date: 1977-01 Impact factor: 4.438

9. Secondary constrictions and nucleolus organizer regions in man.

Authors: M Ferraro; N Archidiacono; F Pelliccia; M Rocchi; A Rocchi; A de Capoa
Journal: Exp Cell Res Date: 1977-02 Impact factor: 3.905

10. An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes.

Authors: S E Bloom; C Goodpasture
Journal: Hum Genet Date: 1976-10-28 Impact factor: 4.132

7 in total

Review 1. Centric fission--simple and complex mechanisms.

Authors: Jo Perry; Howard R Slater; K H Andy Choo
Journal: Chromosome Res Date: 2004 Impact factor: 5.239

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

Review 3. Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors: P Jalbert; B Sele
Journal: J Med Genet Date: 1979-12 Impact factor: 6.318

4. X chromosome replication patterns in a case of X;9 balanced translocation.

Authors: G Filippi; V Pecile; N Archidiacono; E Baragino; G Auber; M Rocchi
Journal: J Med Genet Date: 1983-12 Impact factor: 6.318

5. Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.

Authors: J M Varley; J Gosden; M Hultén
Journal: Hum Genet Date: 1981 Impact factor: 4.132

6. Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Authors: P Jalbert; B Sele; H Jalbert
Journal: Hum Genet Date: 1980 Impact factor: 4.132

7. Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus.

Authors: V G Dev; J Byrne; G Bunch
Journal: Hum Genet Date: 1979-10-02 Impact factor: 4.132

7 in total