Literature DB >> 5091263

The question of trisomy 22 syndrome.

R M Goodman, M B Katznelson, M Spero, R Shaki, B Padeh, N Sadan.   

Abstract

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Year:  1971        PMID： 5091263     DOI： 10.1016/s0022-3476(71)80096-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  7 in total

1.  Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy.

Authors:  P Saldaña-Garcia
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

2.  Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.

Authors:  B S Emanuel; E H Zackai; M M Aronson; W J Mellman; P S Moorhead
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

3.  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

4.  47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.

Authors:  E Kessel; R A Pfeiffer
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

Review 5.  Genetics of the +p9 syndrome.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

6.  A case of trisomy 22 with a probable Robertsonian translocation 21/22.

Authors:  S Lalchev; M Tzancheva; R Markova
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

7.  Trisomy 22. Two new cases and delineation of the phenotype.

Authors:  V B Penchaszadeh; R Coco
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318
  7 in total

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