Literature DB >> 21567909

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

Amy M Breman1, Frank J Probst, Maria A Blazo, Christian P Schaaf, Erin K Roney, William J Craigen, Carlos A Bacino, Sau Wai Cheung.   

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Year:  2011        PMID: 21567909      PMCID: PMC3651890          DOI: 10.1002/ajmg.a.33935

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


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  5 in total

1.  A new trisomic syndrome.

Authors:  J H EDWARDS; D G HARNDEN; A H CAMERON; V M CROSSE; O H WOLFF
Journal:  Lancet       Date:  1960-04-09       Impact factor: 79.321

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

Authors:  A M Vianna-Morgante; M J Nozaki; C C Ortega; V Coates; Y Yamamura
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

3.  Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathology.

Authors:  U Froster-Iskenius; W Coerdt; H Rehder; E Schwinger
Journal:  Clin Genet       Date:  1984-12       Impact factor: 4.438

4.  Features of trisomy 18 and 18p- syndromes in an infant with 45,XY,i(18q).

Authors:  H N Bass; R S Sparkes; A A Miller
Journal:  Clin Genet       Date:  1979-09       Impact factor: 4.438

5.  DNA studies of mono- and pseudodicentric isochromosomes 18q.

Authors:  Merete Bugge; Carsten A Brandt; Michael B Petersen
Journal:  Am J Med Genet A       Date:  2004-06-15       Impact factor: 2.802

  5 in total

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