Literature DB >> 1218221

Trisomy 22: a clinically identifiable syndrome.

O S Alfi, R G Sanger, G M Donnell.   

Abstract

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Mesh：

Year:  1975        PMID： 1218221

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  5 in total

1.  Confirmation of trisomy 22 by trypsin-giemsa staining.

Authors:  M L Begleiter; P Kulkarni; D J Harris
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

2.  Complex chromosomal rearrangement leading to partial trisomy 22.

Authors:  I L Hansteen; L Schirmer; S Hestetun; A Brøgger
Journal:  J Med Genet       Date:  1980-02       Impact factor: 6.318

3.  Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

Authors:  A Schinzel; W Schmid; P Auf der Maur; H Moser; K H Degenhardt; M Geisler; A Grubisic
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Hydrocephalus in an infant with trisomy 22.

Authors:  F Fahmi; S Schmerler; R G Hutcheon
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

5.  Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.

Authors:  Melissa T Carter; Stephanie A St Pierre; Elaine H Zackai; Beverly S Emanuel; Kym M Boycott
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802
  5 in total

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