Literature DB >> 4117153

Dicentric and monocentric Robertsonian translocations in man.

E Niebuhr.   

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Year:  1972        PMID： 4117153     DOI： 10.1007/bf00273467

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  17 in total

1.  Localization of heterochromatin in human chromosomes.

Authors:  F E Arrighi; T C Hsu
Journal:  Cytogenetics       Date:  1971

2.  Human chromosome identification by differential staining: G goup (21-22-Y).

Authors:  P R Chernay; L Y Hsu; H Streicher; K Hirschhorn
Journal:  Cytogenetics       Date:  1971

3.  Constitutive heterochromatin patterns of G-group chromosomes in Down's syndrome.

Authors:  S Pathak; A K Sinha
Journal:  Humangenetik       Date:  1972

4.  Identification of human chromosomes by DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson; E J Modest
Journal:  Chromosoma       Date:  1970       Impact factor: 4.316

5.  A 45,XX,5-,13-,dic+ karyotype in a case of cri-du-chat syndrome.

Authors:  E Niebuhr
Journal:  Cytogenetics       Date:  1972

6.  Trisomy D1 with two D-D translocation chromosomes. Report of a case.

Authors:  M M Cohen; N Takagi; E K Harrod
Journal:  Am J Dis Child       Date:  1968-02

7.  Chromosomal localization of mouse satellite DNA.

Authors:  M L Pardue; J G Gall
Journal:  Science       Date:  1970-06-12       Impact factor: 47.728

8.  Dicentric chromosome due to an unusual fusion.

Authors:  I Subrt; B Blehová; O Táborský
Journal:  Humangenetik       Date:  1971

9.  Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.

Authors:  T Caspersson; M Hultén; J Lindsten; A J Therkelsen; L Zech
Journal:  Hereditas       Date:  1971       Impact factor: 3.271

10.  The fluorescence pattern of the human karyotype.

Authors:  G Manolov; Y Manolova; A Levan
Journal:  Hereditas       Date:  1971       Impact factor: 3.271
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  38 in total

1.  Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions.

Authors:  L M Farah; H R de Nazareth; M Dolnikoff; D Delascio
Journal:  Humangenetik       Date:  1975-08-25

2.  Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome.

Authors:  T Abe; M Morita; K Kawai; S Misawa; H Kanai; G Hirose; H Fujita
Journal:  Humangenetik       Date:  1975-09-20

3.  Delineation of Robertsonian translocations in man by means of chromosome banding.

Authors:  F S Hill; R L Summitt
Journal:  Eur J Pediatr       Date:  1977-11-04       Impact factor: 3.183

4.  Structure and inheritance of some heterozygous Robertsonian translocation in man.

Authors:  A Daniel; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

5.  Dicentric X isochromosomes in man.

Authors:  R T Howell; S H Roberts; R J Beard
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

6.  Centromere activity in dicentric small supernumerary marker chromosomes.

Authors:  Elisabeth Ewers; Kinya Yoda; Ahmed B Hamid; Anja Weise; Marina Manvelyan; Thomas Liehr
Journal:  Chromosome Res       Date:  2010-06-22       Impact factor: 5.239

7.  Characterization of Robertsonian translocations by using fluorescence in situ hybridization.

Authors:  D J Wolff; S Schwartz
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

8.  Evolutionary histories of highly repeated DNA families among the Artiodactyla (Mammalia).

Authors:  W S Modi; D S Gallagher; J E Womack
Journal:  J Mol Evol       Date:  1996-03       Impact factor: 2.395

9.  Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.

Authors:  B A Sullivan; L S Jenkins; E M Karson; J Leana-Cox; S Schwartz
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

10.  Causes and consequences of Robertsonian exchange.

Authors:  B John; M Freeman
Journal:  Chromosoma       Date:  1975-09-26       Impact factor: 4.316
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