Summary
We describe a case of (2) (q34;q36) deletion in a girl. The main clinical features of the proband are staturo-ponderal retardation, skull-face dysmorphia and an interauricular communication. The relationship between morphological and chromosomal abnormalities is discussed.
Article PDF
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Bibliographie
German, J., Chaganti, R. S. K.: Mapping human autosomes: Assignement of the MN locus to a specific segment in the long arm of chromosome no. 2. Science 182, 1261–1262 (1973)
German, J., Walker, M. E., Stiefel, F. H., Allen, F. H.: MN blood-group locus: Data concerning the possible chromosomal location. Science 162, 1014–1015 (1968)
Seabright, M.: The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man. Chromosoma (Berl.) 36, 204–210 (1972)
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Warter, S., Lausecker, C. & Pennerath, A. Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2) (q34q36). Hum Genet 32, 225–227 (1976). https://doi.org/10.1007/BF00291510
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00291510