Literature DB >> 5517331

[Tendency for chromosome breaks in Russel's syndrome].

E Ganner, A Schwingshackl.   

Abstract

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Year:  1970        PMID： 5517331     DOI： 10.1007/bf01485398

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN： 0023-2173


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  27 in total

1.  ASYMMETRY, SHORT STATURE, AND VARIATIONS IN SEXUAL DEVELOPMENT. A SYNDROME OF CONGENITAL MALFORMATIONS.

Authors:  H K SILVER
Journal:  Am J Dis Child       Date:  1964-05

2.  Low birth weight dwarfism.

Authors:  J BLACK
Journal:  Arch Dis Child       Date:  1961-12       Impact factor: 3.791

3.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

4.  INTRAUTERINE GROWTH RETARDATION VERSUS SILVER'S SYNDROME.

Authors:  G C SZALAY
Journal:  J Pediatr       Date:  1964-02       Impact factor: 4.406

5.  Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia.

Authors:  J C Jacobs; A de Capoa; E McGilvray; J H Morse; J N Schullinger; W A Blanc; W C Heird; O J Miller; R D Rossen; R A Walzer
Journal:  Lancet       Date:  1968-03-09       Impact factor: 79.321

6.  [The Russell dwarf: a rare form of dwarfism with prior retarded growth in utero].

Authors:  J Girard; H J Kaufmann
Journal:  Monatsschr Kinderheilkd       Date:  1965-12

7.  Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth.

Authors:  A Sawitsky; D Bloom; J German
Journal:  Ann Intern Med       Date:  1966-09       Impact factor: 25.391

8.  [Cytogenetic finding and etiology of Fanconi's anemia. A case of Fanconi's anemia without hexokinase deficiency].

Authors:  T M Schroeder
Journal:  Humangenetik       Date:  1966

9.  [Biochemical defects in the blood cells in familial panmyelopathy (Fanconi type)].

Authors:  G W Löhr; H D Waller; F Anschütz; A Knopp
Journal:  Humangenetik       Date:  1965

10.  Silver's syndrome: report of a case with chromosomal and dermatoglyphic study.

Authors:  P E Ferrier; S A Ferrier
Journal:  J Pediatr       Date:  1967-03       Impact factor: 4.406
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  1 in total

1.  [Basal cell nevus syndrome with retinopathia pigmentosa, recurrent vitreous body hemorrhage and chromosome aberrations].

Authors:  R Happle; G Mehrle; L Z Sander; H Höhn
Journal:  Arch Dermatol Forsch       Date:  1971
  1 in total

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