Literature DB >> 1150241

Three cases of minor chromosomal aberrations discovered by prenatal chromosome determination.

J Wahlström.   

Abstract

A case of pronounced secondary constriction of a chromosome belonging to pair N0. 9, a case of deletion of the short arms of one of the chromosomes in pair No. 13, and a case of partial trisomy of the distal portion of a chromosome in pair No. 14 were discovered by prenatal chromosome determination. Analysis of the parents' karyotypes enabled the clinical importance of the three different chromosomal aberrations to be elucidated.

Mesh：

Year:  1975        PMID： 1150241     DOI： 10.1007/bf00278348

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


  3 in total

1.  CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

Authors:  J L HAMERTON; F GIANNELLI; P E POLANI
Journal:  Cytogenetics       Date:  1965

2.  Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson; E Zeuthen
Journal:  Humangenetik       Date:  1974

3.  A prenatally discovered unbalanced translocation t(14;22) (q22 or 23;q13).

Authors:  J WAHLSTROM
Journal:  Hereditas       Date:  1974       Impact factor: 3.271
  3 in total

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