Literature DB >> 5643178

Familial occurrence of trisomy 22.

I A Uchida, M Ray, K N McRae, D F Besant.   

Abstract

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Year:  1968        PMID： 5643178      PMCID： PMC1706268     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  16 in total

1.  Another child with 47 chromosomes.

Authors:  J FERGUSON; D PITT
Journal:  Med J Aust       Date:  1963-04-13       Impact factor: 7.738

2.  A familial chromosome abnormality associated with repeated abortions.

Authors:  W SCHMID
Journal:  Cytogenetics       Date:  1962

3.  An apparently identical extra autosome in two severely retarded sisters with multiple malformations.

Authors:  K H GUSTAVSON; B HAGBERG; S C FINLEY; W H FINLEY
Journal:  Cytogenetics       Date:  1962

4.  [Apropos of a case of 22-trisomy].

Authors:  L KOULISCHER; J PERIER
Journal:  Bull Acad R Med Belg       Date:  1962

5.  An air-drying technique for flattening chromosomes in mammalian oells grown in vitro.

Authors:  K H ROTHFELS; L SIMINOVITCH
Journal:  Stain Technol       Date:  1958-03

6.  XO-XX-XXX mosaicism with Turner stigmata.

Authors:  J Antich; M Ribas-Mundo; J Prats; J M Frances
Journal:  Lancet       Date:  1967-06-03       Impact factor: 79.321

7.  An extra chromosome in a case of Tay-Sachs disease with additional abnormalities.

Authors:  P L Giorgi; A Paci; M Ceccarelli
Journal:  Helv Paediatr Acta       Date:  1967-04

8.  A child with an extra small metacentric chromosome.

Authors:  M D Crawfurd; K P Lele
Journal:  Ann Hum Genet       Date:  1965-11       Impact factor: 1.670

9.  The first arch syndrome.

Authors:  J McKenzie
Journal:  Dev Med Child Neurol       Date:  1966-02       Impact factor: 5.449

10.  Chromosome studies on randomly chosen men and women.

Authors:  W M Brown; P A Jacobs; M Brunton
Journal:  Lancet       Date:  1965-09-18       Impact factor: 79.321
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  15 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.  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

4.  Trisomy 22 mosaicism.

Authors:  F Mollica; G Sorge; L Pavone
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

5.  Short arm enlargement in acrocentric chromosomes.

Authors:  V E Sands
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

6.  Additional G-like chromosome in a malformed boy.

Authors:  M Fraccaro; M Hultén; S D Jayakar; A Lindsjö; J Lindsten; L Tiepolo
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

7.  Aneuploidy of the chromosome G(21-22) autosomes. Current concepts.

Authors:  S Hara; E P Crump
Journal:  J Natl Med Assoc       Date:  1971-07       Impact factor: 1.798

8.  Morphology alone does not make an isochromosome.

Authors:  S M Schmutz; E Pinno
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

Review 9.  Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism.

Authors:  E M Kuhn; G E Sarto; B J Bates; E Therman
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

10.  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
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