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Analysis of crossing-over in a family with translocation 9;10 involving a chromosome 9 with a pericentric inversion

✍ Scribed by J. H. Priest; D. K. Lavett; J. P. Marion

Publisher
Springer
Year
1985
Tongue
English
Weight
379 KB
Volume
71
Category
Article
ISSN
0340-6717

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A girl with 46, XX, de1 (11) (q23), inv (9) (p13,q13) is described. The patient shows many dysplastic signs mainly of the face and skull. The pericentric inversion of chromosome 9 has been inherited from the mother (46, XX, inv (9) (p13,q13)).