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Literature DB >> 631845

A fetus with recombinant of chromosome 8 inherited from her carrier father.

A Fujimoto, J W Towner, S B Turkel, M G Wilson.

Abstract

A pericentric inversion of chromosome 8, inv(8)(p23q22), in a male carrier resulted in an unbalanced recombinant, rec(8)dup q, inv(8)(p23q22), which was diagnosed prenatally. The features seen in the aborted fetus resembled the features seen in a previously affected child who received the identical recombinant from her carrier mother. In this particular inversion involving chromosome 8, both male and female carriers risk producing an unbalanced progeny. Different familial pericentric inversions are reviewed for the presence or absence of unbalanced recombinants.

Entities: Chemical Species

Mesh：

Year: 1978 PMID： 631845 DOI： 10.1007/bf00272184

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

33 in total

1. Inversion homozygosity of chromosome no. 9 in a higly inbred kindred.

Authors: D T Vine; S Yarkoni; M M Cohen
Journal: Am J Hum Genet Date: 1976-05 Impact factor: 11.025

2. [Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].

Authors: B Dallapiccola; L Capra; G Preto; M Covic; B Dutrillaux
Journal: Ann Genet Date: 1974-06

3. Trisomy 8.

Authors: L Atkins; L B Holmes; V M Riccardi
Journal: J Pediatr Date: 1974-02 Impact factor: 4.406

4. Pericentric inversion of chromosome 9.

Authors: D E Mutton; M G Daker
Journal: Nat New Biol Date: 1973-01-17

5. Down's syndrome with an atypical G-G translocation derived from familial pericentric inversion in one chromosome of the G group.

Authors: S Morić-Petrović; Z Laća; P Kalicanin
Journal: J Med Genet Date: 1972-12 Impact factor: 6.318

6. Pericentric Y inversion in the general population.

Authors: E Zeuthen; J Nielsen
Journal: Humangenetik Date: 1973-09-20

7. Pericentric inversions of chromosome 9 in two families.

Authors: J Wahrman; J Atidia; R Goitein; T Cohen
Journal: Cytogenetics Date: 1972

8. Inherited pericentric inversion of chromosome number two: a linkage study.

Authors: L R Weitkamp; M K Janzen; S A Guttormsen; H Gershowitz
Journal: Ann Hum Genet Date: 1969-07 Impact factor: 1.670

9. An inherited pericentric chromosomal inversion (46, inv3 (p-q+)) associated with skeletal anomalies.

Authors: M M Cohen; R G Davidson
Journal: J Pediatr Date: 1971-09 Impact factor: 4.406

10. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

Authors: P W Allderdice; N Browne; D P Murphy
Journal: Am J Hum Genet Date: 1975-11 Impact factor: 11.025

9 in total

1. Review of radiologic and clinical findings in the recombinant 8 syndrome.

Authors: S L Williamson; C L Clericuzio
Journal: Pediatr Radiol Date: 1991

2. Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States.

Authors: A C Smith; K Spuhler; T M Williams; T McConnell; E Sujansky; A Robinson
Journal: Am J Hum Genet Date: 1987-12 Impact factor: 11.025

A fetus with recombinant of chromosome 8 inherited from her carrier father.

1. Inversion homozygosity of chromosome no. 9 in a higly inbred kindred.

2. [Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].

3. Trisomy 8.

4. Pericentric inversion of chromosome 9.

5. Down's syndrome with an atypical G-G translocation derived from familial pericentric inversion in one chromosome of the G group.

6. Pericentric Y inversion in the general population.

7. Pericentric inversions of chromosome 9 in two families.

8. Inherited pericentric inversion of chromosome number two: a linkage study.

9. An inherited pericentric chromosomal inversion (46, inv3 (p-q+)) associated with skeletal anomalies.

10. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

1. Review of radiologic and clinical findings in the recombinant 8 syndrome.

2. Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States.

3. A child with a recombinant of chromosome 8 inherited from her carrier mother.

4. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.

5. Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).

6. Prenatal diagnosis by amniocentesis in 800 pregnancies.

7. Duplication deficiency as the result of meiotic segregation of a maternal InV (10).

8. Pericentric inversions in man: personal experience and review of the literature.

9. Chromosomal analysis of couples with repeated spontaneous abortions in northeastern iran.