Literature DB >> 1003448

Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.

A M Vianna-Morgante, M J Nozaki, C C Ortega, V Coates, Y Yamamura.   

Abstract

A pericentric inversion of chromosome 18 is described in the mother of a patient with clinical diagnosis of 18q--syndrome. The propositus' chromosome complement includes the recombinant 18 with deficiency of the distal one-third of the long arm and duplication of the terminal segment of the short arm. The propositus' sister carrier the recombinant 18 with a duplication of the distal one-third of the long arm and a deficiency of the terminal segment of the short arm. The relative length of the inverted segment represents about 60% of the total chromosome 18 length. The probability of recombinant formation following the occurrence of a chiasma within the inverted segment is predicted to be high.

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Year:  1976        PMID: 1003448      PMCID: PMC1013442          DOI: 10.1136/jmg.13.5.366

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  14 in total

1.  Pericentric inversion of "fluorescent" segment in chromosome no. 3.

Authors:  D Soudek; S O'Shaughnessy; P Laraya; B D McCreary
Journal:  Humangenetik       Date:  1974

2.  Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.

Authors:  M J Faed; V J Marrian; J Robertson; E B Robson; P J Cook
Journal:  Cytogenetics       Date:  1972

3.  A cytogenetic survey of 11,680 newborn infants.

Authors:  P A Jacobs; M Melville; S Ratcliffe; A J Keay; J Syme
Journal:  Ann Hum Genet       Date:  1974-05       Impact factor: 1.670

4.  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

5.  Karyotype with chromosomal abnormality with various inherited defects in the offspring (recombination aneusomy).

Authors:  S Warter; J V Ruch; M Lehmann
Journal:  Humangenetik       Date:  1973-12-20

6.  Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.

Authors:  H Hauksdóttir; S Halldórsson; O Jensson; M Mikkelsen; A McDermott
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

7.  Inherited pericentric inversion of a group D (13-15) chromosome.

Authors:  R B Surana; P E Conen
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

8.  Pericentric inversions of chromosome 9 in two families.

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

9.  Pericentric inversion of a number 15 chromosome in nine members of one family.

Authors:  B F Crandall; R S Sparkes
Journal:  Cytogenetics       Date:  1970

10.  The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.

Authors:  T Caspersson; G Lomakka; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

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  14 in total

1.  Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.

Authors:  Amy M Breman; Frank J Probst; Maria A Blazo; Christian P Schaaf; Erin K Roney; William J Craigen; Carlos A Bacino; Sau Wai Cheung
Journal:  Am J Med Genet A       Date:  2011-05-12       Impact factor: 2.802

2.  Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18.

Authors:  V Vigi; P Maraschio; G Bosi; P Guerini; M Fraccaro
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

3.  A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria.

Authors:  Julio A Poterico; Flor Vásquez; Miguel Chávez-Pastor; Milana Trubnykova; Félix Chavesta; Jenny Chirinos; Nancy Salcedo; Rosmery Mena; Sulema Cubas; Rocío González; Rossana Alvariño; Hugo Abarca-Barriga
Journal:  J Pediatr Genet       Date:  2017-07-06

4.  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

5.  A homozygote for pericentric inversion of chromosome 4.

Authors:  N J Carpenter; B Say; N D Barber
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

6.  Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling.

Authors:  J R Teyssier; F Bajolle
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

Review 7.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Four families with immunodeficiency and chromosome abnormalities.

Authors:  D C Candy; A R Hayward; D T Hughes; L Layward; J F Soothill
Journal:  Arch Dis Child       Date:  1979-07       Impact factor: 3.791

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

Authors:  E Yunis; O Torres de Caballero
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  Trisomy 18q. A case report and review of karyotype-phenotype correlations.

Authors:  R Matsuoka; S Matsuyama; Y Yamamoto; Y Kuroki; I Matsui
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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