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Page 1
A review of Klinefelter's syndrome in children and adolescents.
Mandoki MW, Sumner GS, Hoffman RP, Riconda DL. Mandoki MW, et al. Among authors: riconda dl. J Am Acad Child Adolesc Psychiatry. 1991 Mar;30(2):167-72. doi: 10.1097/00004583-199103000-00001. J Am Acad Child Adolesc Psychiatry. 1991. PMID: 2016217 Review.
Maternal serum alphafetoprotein screening. University Medical Center.
Morris N, Riconda D, Marfatia L, Ostrer H. Morris N, et al. J Fla Med Assoc. 1991 Jun;78(6):365-8. J Fla Med Assoc. 1991. PMID: 1714937
Restoration of half the normal dystrophin sequence in a double-deletion Duchenne muscular dystrophy family.
Hoop RC, Russo LS, Riconda DL, Schwartz LS, Hoffman EP. Hoop RC, et al. Among authors: riconda dl. Am J Med Genet. 1994 Feb 1;49(3):323-7. doi: 10.1002/ajmg.1320490316. Am J Med Genet. 1994. PMID: 8209894
Genetic counselor training for the next generation: Where do we go from here?
Riconda D, Grubs RE, Campion MW, Cragun D. Riconda D, et al. Am J Med Genet C Semin Med Genet. 2018 Mar;178(1):38-45. doi: 10.1002/ajmg.c.31598. Epub 2018 Mar 7. Am J Med Genet C Semin Med Genet. 2018. PMID: 29512933 No abstract available.
Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15.
Cheung SW, Shaffer LG, Richards CS, Page SL, Riconda DL. Cheung SW, et al. Among authors: riconda dl. Am J Med Genet. 1997 Oct 3;72(1):47-50. doi: 10.1002/(sici)1096-8628(19971003)72:1<47::aid-ajmg10>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9295074
Features of Multiple Endocrine Neoplasia Type 1 and 2A in a Patient with Both RET and MEN1 Germline Mutations.
Brown SJ, Riconda DL, Zheng F, Jackson GL, Suo L, Robbins RJ. Brown SJ, et al. Among authors: riconda dl. J Endocr Soc. 2020 Feb 18;4(4):bvaa020. doi: 10.1210/jendso/bvaa020. eCollection 2020 Apr 1. J Endocr Soc. 2020. PMID: 32190804 Free PMC article.