Literature DB >> 4976446

[A female patient with translocation 46, XX, t(Dq-; Bq+) and neurofibromatosis, imbecility and aortic coarctation].

E Ganner.   

Abstract

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Year:  1969        PMID： 4976446

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN： 0036-7672


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  3 in total

1.  Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study.

Authors:  H J Decker; L A Cannizzaro; M J Mendez; S P Leong; H Bixenman; C Berger; A A Sandberg
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

2.  [Tandem chromosome (G-G) with satellites on short and long arm in a patient with trisomy G1].

Authors:  W Vogel; H Reinwein; W Engel
Journal:  Humangenetik       Date:  1970

3.  [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
  3 in total

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