Cited by

• Meiotic recombination in the beta globin gene cluster causing an error in prenatal diagnosis of beta thalassaemia.

  Camaschella C, Serra A, Saglio G, Bertero MT, Mazza U, Terzoli S, Brambati B, Cremonesi L, Travi M, Ferrari M. Camaschella C, et al. J Med Genet. 1988 May;25(5):307-10. doi: 10.1136/jmg.25.5.307. J Med Genet. 1988. PMID: 2898535 Free PMC article.
• Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.

  Panny SR, Scott AF, Smith KD, Phillips JA 3rd, Kazazian HH Jr, Talbot CC Jr, Boehm CD. Panny SR, et al. Am J Hum Genet. 1981 Jan;33(1):25-35. Am J Hum Genet. 1981. PMID: 6162380 Free PMC article.
• Haplotype analysis of familial amyloidotic polyneuropathy. Evidence for multiple origins of the Val----Met mutation most common to the disease.

  Yoshioka K, Furuya H, Sasaki H, Saraiva MJ, Costa PP, Sakaki Y. Yoshioka K, et al. Hum Genet. 1989 Apr;82(1):9-13. doi: 10.1007/BF00288262. Hum Genet. 1989. PMID: 2714785
• Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster.

  Chakravarti A, Phillips JA 3rd, Mellits KH, Buetow KH, Seeburg PH. Chakravarti A, et al. Proc Natl Acad Sci U S A. 1984 Oct;81(19):6085-9. doi: 10.1073/pnas.81.19.6085. Proc Natl Acad Sci U S A. 1984. PMID: 6091133 Free PMC article.
• Genetic and molecular analysis of familial isolated growth hormone deficiency.

  Ruiz-Pacheco R, Chatelain P, Sizonenko PC, Bost M, Garandau P, Sultan C. Ruiz-Pacheco R, et al. Hum Genet. 1993 Oct 1;92(3):273-81. doi: 10.1007/BF00244472. Hum Genet. 1993. PMID: 8104861