Literature DB >> 14458605

[Chromosomal aberrations and their clinical significance].

W KOSENOW, R A PFEIFFER.   

Abstract

Keywords:  CHROMOSOMES

Mesh：

Year:  1962        PMID： 14458605     DOI： 10.1055/s-0028-1112082

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN： 0012-0472            Impact factor:   0.628


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  7 in total

1.  [CHROMOSOME MOSAIC 45/XO-/46XX-/47/XXX SIMULATING A "TRUE GONADAL DYSGENESIS"].

Authors:  R ZABEL; R WITKOWSKI; J DAMM
Journal:  Arch Klin Exp Dermatol       Date:  1964-05-15

Review 2.  [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY].

Authors:  O HORNSTEIN
Journal:  Arch Klin Exp Dermatol       Date:  1963-09-02

3.  [ON THE CYTOGENETICS OF DIFFERENT GENODERMATOSES AND ABNORMALITY SYNDROMES].

Authors:  O HORNSTEIN
Journal:  Arch Klin Exp Dermatol       Date:  1964-06-25

4.  [FAMILIAL OCCURRENCE OF OSTEOGENESIS IMPERFECTA TARDA. OBSERVATIONS ON 4 GENERATIONS].

Authors:  G KLEMM; F D KLEINE; R WITKOWSKI; L LACHHEIN
Journal:  Klin Wochenschr       Date:  1965-01-01

5.  [Chromosome changes in acute intermittent porphyria].

Authors:  U Burchardt; T Wichmann; K Zernahle
Journal:  Klin Wochenschr       Date:  1968-04-15

6.  [Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].

Authors:  T M Schroeder
Journal:  Humangenetik       Date:  1966

7.  [Spontaneous chromosome aberrations in familial panmyelopathy].

Authors:  T M Schroeder; F Anschütz; A Knopp
Journal:  Humangenetik       Date:  1964
  7 in total

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