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Di George syndrome and 22q11 rearrangements

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References

  • De La Chapelle A, Herva R, Koivisto M, Aula P (1981) A deletion in chromosome 22 can cause Di George syndrome. Hum Genet 57:253–256

    Google Scholar 

  • Kelley RI, Zackai EH, Emanuel BS, Kistenmacher M, Greenberg F, Punnett HH (1982) The association of the Di George anomalad with partial monosomy of chromosome 22. J Pediatr 101:197–200

    Google Scholar 

  • Greenberg F, Crowder WE, Paschall V, Colon-Linares J, Lubianski B, Ledbetter DH (1984) Familial Di George syndrome and associated partial monosomy of chromosome 22. Hum Genet 65:317–319

    Google Scholar 

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Augusseau, S., Jouk, S., Jalbert, P. et al. Di George syndrome and 22q11 rearrangements. Hum Genet 74, 206 (1986). https://doi.org/10.1007/BF00282098

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