Literature DB >> 4646558

Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease.

M Faed, H G Morton, J Robertson.   

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Year:  1972        PMID： 4646558      PMCID： PMC1469060          DOI： 10.1136/jmg.9.4.470

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


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  12 in total

1.  Chromosomal aberrations in acute leukemia.

Authors:  K A Kiossoglou; W J Mitus; W Dameshek
Journal:  Blood       Date:  1965-11       Impact factor: 22.113

2.  [Chromosome analyses in idiopathic acquired sideroblastic anemia. A study of 6 cases].

Authors:  J de Grouchy; C de Nava; R Zittoun; J Bousser
Journal:  Nouv Rev Fr Hematol       Date:  1966 May-Jun

3.  [Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation].

Authors:  G Loiodice; D G Rovetta; G Bellicini; G Callura; F Bergamo
Journal:  Minerva Pediatr       Date:  1970-05-26       Impact factor: 1.312

4.  Long-arm deletion of 19-20 chromosomes.

Authors:  M Ahmed
Journal:  Lancet       Date:  1972-02-19       Impact factor: 79.321

5.  Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient.

Authors:  P Genest; M Bouchard; J Poty
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

6.  Partial F trisomy and parental chromosomes.

Authors:  R S Sparkes; R E Carrel; S W Wright
Journal:  Lancet       Date:  1968-08-17       Impact factor: 79.321

7.  Chromosome abnormalities in two cases with bilateral radial element defects.

Authors:  M Faed; A Stewart; A J Keay
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

8.  Further observations on patients with a chromosomal abnormality associated with polycythaemia vera.

Authors:  R E Millard; S D Lawler; H E Kay; C B Cameron
Journal:  Br J Haematol       Date:  1968-04       Impact factor: 6.998

9.  Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson
Journal:  Exp Cell Res       Date:  1970-10       Impact factor: 3.905

10.  Unusual chromosomal findings in a case of myelofibrosis.

Authors:  R M Goodman; B A Bouroncle; F Miller; C North
Journal:  J Hered       Date:  1968 Nov-Dec       Impact factor: 2.645
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  7 in total

1.  Deletion of the short arms of chromosome 20.

Authors:  D K Kalousek; S Thérien
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

2.  Cognitive impairment and abnormal behaviour related to ring chromosome 20 aberration.

Authors:  Maximilian Gahr; Frank Kerling; Andrea Ludolph; Paul Plener
Journal:  J Autism Dev Disord       Date:  2012-06

3.  The r(20) syndrome.

Authors:  R Herva; I Saarinen; L Leikkonen
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

4.  Trisomy for short arm of chromosome 20.

Authors:  I Subrt; V Brychnác
Journal:  Humangenetik       Date:  1974

5.  Familial ring (20) chromosomal mosaicism.

Authors:  E Back; I Voiculescu; M Brünger; G Wolff
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

6.  Ring 20 chromosome in a child with seizures, minor anomalies, and retardation.

Authors:  J M Stewart; N Cavanagh; D T Hughes
Journal:  Arch Dis Child       Date:  1979-06       Impact factor: 3.791

Review 7.  Epileptic syndromes: From clinic to genetic.

Authors:  Abbas Tafakhori; Vajiheh Aghamollaii; Sara Faghihi-Kashani; Payam Sarraf; Laleh Habibi
Journal:  Iran J Neurol       Date:  2015-01-05
  7 in total

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