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.
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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
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DOI: https://doi.org/10.1007/BF00291510