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1978 1
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Page 1
A 45,X/69,XXY fetus.
Betts DR, Fear CN, Barby T, Seller MJ. Betts DR, et al. Among authors: fear cn. Clin Genet. 1989 Apr;35(4):285-8. doi: 10.1111/j.1399-0004.1989.tb02945.x. Clin Genet. 1989. PMID: 2714016
Two cases of interstitial deletion 1p.
Lai MM, Robards MF, Berry AC, Fear CN, Hart C. Lai MM, et al. Among authors: fear cn. J Med Genet. 1991 Feb;28(2):128-30. doi: 10.1136/jmg.28.2.128. J Med Genet. 1991. PMID: 2002484 Free PMC article.
Fragile X in a normal male: a cautionary tale.
Daker MG, Chidiac P, Fear CN, Berry AC. Daker MG, et al. Among authors: fear cn. Lancet. 1981 Apr 4;1(8223):780. doi: 10.1016/s0140-6736(81)92652-0. Lancet. 1981. PMID: 6110980 No abstract available.
A 1q translocation family segregating for peptidase C.
Cook PJ, Fear CN, Povey S. Cook PJ, et al. Among authors: fear cn. Cytogenet Cell Genet. 1978;22(1-6):375-7. doi: 10.1159/000130975. Cytogenet Cell Genet. 1978. PMID: 752507 No abstract available.
Chromosome 15 in Prader-Willi syndrome.
Fear CN, Mutton DE, Berry AC, Heckmatt JZ, Dubowitz V. Fear CN, et al. Dev Med Child Neurol. 1985 Jun;27(3):305-11. doi: 10.1111/j.1469-8749.1985.tb04540.x. Dev Med Child Neurol. 1985. PMID: 4018424 Free PMC article.