Literature DB >> 4142012

Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.

T Caspersson, M Hultén, J Jonasson, J Lindsten, A Therkelsen, L Zech.   

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Year:  1971        PMID： 4142012     DOI： 10.1111/j.1601-5223.1971.tb02407.x

Source DB:  PubMed          Journal:  Hereditas        ISSN： 0018-0661            Impact factor:   3.271


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  21 in total

1.  The occurrence of gonadal dysgenesis in association with monozygotic twinning.

Authors:  L Karp; J I Bryant; G Tagatz; E Giblett; P J Fialkow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

Authors:  F Speleman; B Van der Auwera; K Mangelschots; M Vercruyssen; T Raap; J Wiegant; M Craen; J Leroy
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  X/XYq - mosaicism and mixed gonadal dysgenesis.

Authors:  E Yunis; R Silva; E Ramirez; M A Nossa
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

4.  Three cases of sex chromosome mosaicism with a nonfluorescent Y.

Authors:  K Madan; L Gooren; J Schoemaker
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

5.  A phenotypically Turner-like female with karyotype 45,X/46,XY, gonadoblastoma and fluorescent Y.

Authors:  A Serra; E Moneta; V Patrono; G Pizzolato
Journal:  Humangenetik       Date:  1974

6.  A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres.

Authors:  D Warburton; A S Henderson; L R Shapiro; L Y Hsu
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

7.  Human dicentric Y chromosomes. Case report and review of the literature.

Authors:  M M Cohen; M H MacGillivray; V J Capraro; T A Aceto
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

8.  Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf).

Authors:  D Gänshirt; I H Pawlowitzki
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Prenatal diagnosis of a de novo Y/22 translocation.

Authors:  M Verjaal; P E Treffers; Y Nagal; N J Leschot
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

10.  45,X/46,XY mosaicism. A clinical review and report of ten cases.

Authors:  J Knudtzon; D Aarskog
Journal:  Eur J Pediatr       Date:  1987-05       Impact factor: 3.183
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