Literature DB >> 4957345

Structural (translocation) heterozygosity over three subsequent generations in man.

A Gropp, W Marsch, J Brodehl.   

Abstract

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Year:  1965        PMID： 4957345     DOI： 10.1038/207374a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  3 in total

1.  [CHROMOSOME ANOMALIES IN MALFORMATION SYNDROMES (SO-CALLED D-AND E-TRISOMIC SYNDROME)].

Authors:  W MARSCH; A GROPP; H W ROTTHAUWE
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1964-11-09

2.  Familial translocation t(3p+;8q-) studied by banding with giemsa staining.

Authors:  A Del Amo; A Gullón
Journal:  Humangenetik       Date:  1972

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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