Cited by

• Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.

  Roberts SH, Duckett DP. Roberts SH, et al. J Med Genet. 1978 Oct;15(5):375-81. doi: 10.1136/jmg.15.5.375. J Med Genet. 1978. PMID: 739528 Free PMC article.
• Hypogammaglobulinaemia in a patient with ring chromosome 21.

  Ohga S, Nakao F, Narazaki O, Fusazaki N, Aoki T, Kamesaki K, Hara T. Ohga S, et al. Arch Dis Child. 1997 Sep;77(3):252-4. doi: 10.1136/adc.77.3.252. Arch Dis Child. 1997. PMID: 9370908 Free PMC article.
• Full monosomy 21: a clinically recognizable syndrome?

  Fryns JP, D'Hondt F, Goddeeris P, van den Berghe H. Fryns JP, et al. Hum Genet. 1977 Jun 30;37(2):155-9. doi: 10.1007/BF00393578. Hum Genet. 1977. PMID: 885536
• A case of 21q-syndrome with half normal SOD-1 activity.

  Yoshimitsu K, Hatano S, Kobayashi Y, Takeoka Y, Hayashidani M, Ueda K, Nomura K, Ohama K, Usui T. Yoshimitsu K, et al. Hum Genet. 1983;64(2):200-2. doi: 10.1007/BF00327128. Hum Genet. 1983. PMID: 6885062
• Long-arm deletion of chromosome 22, with protein-losing enteropathy.

  Nelson R. Nelson R. Proc R Soc Med. 1972 Dec;65(12):1081-3. doi: 10.1177/003591577206501212. Proc R Soc Med. 1972. PMID: 4651392 Free PMC article. No abstract available.