Literature DB >> 5875584

[Cytogenetic study of a mother and her son presenting the same ocular malformation].

L Koulischer, J Zanen.   

Abstract

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Year:  1964        PMID： 5875584

Source DB:  PubMed          Journal:  Bull Soc Belge Ophtalmol        ISSN： 0081-0746


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  6 in total

1.  Frequency and genetic effect of 1qh plus.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson
Journal:  Humangenetik       Date:  1974-02-21

2.  Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.

Authors:  H Van den Berghe; M Van Eygen; J P Fryns; W Tanghe; H Verresen
Journal:  Humangenetik       Date:  1973-05-25

3.  [Multiple abnormalities in a girl with a 46, XY,17q+ karyotype].

Authors:  W Engel; H Reinwein; D Bombel; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1968

4.  [Elongated, submetacentric chromosome no. 1. A very rare heterozygote variant in man].

Authors:  B Saner
Journal:  Humangenetik       Date:  1970-08-17

5.  Probable pericentric inversion in chromosome no. 1 in a female child (46,XX,inv(Ip+q-).

Authors:  A V Mikelsaar; E V Ananjev; V M Gindilis
Journal:  Humangenetik       Date:  1970

6.  A statistical study of the brachial indices of chromosomes 1,2 and 3, and of an heterozygous abnormality of chromosomes 1.

Authors:  H Galperin
Journal:  Humangenetik       Date:  1966
  6 in total

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