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Thrombocytopenia-absent radius syndrome: a clinical genetic study.
Greenhalgh KL, Howell RT, Bottani A, Ancliff PJ, Brunner HG, Verschuuren-Bemelmans CC, Vernon E, Brown KW, Newbury-Ecob RA. Greenhalgh KL, et al. Among authors: howell rt. J Med Genet. 2002 Dec;39(12):876-81. doi: 10.1136/jmg.39.12.876. J Med Genet. 2002. PMID: 12471199 Free PMC article.
Duplication 2 (q11.2-q21): a previously unreported abnormality.
Cooke LB, Richards H, Lunt PW, Burvill-Holmes L, Howell RT, McDermott A. Cooke LB, et al. Among authors: howell rt. J Med Genet. 1995 Oct;32(10):825-6. doi: 10.1136/jmg.32.10.825. J Med Genet. 1995. PMID: 8558566 Free PMC article.
Terminal deletion of the long arm of chromosome 10.
Curtis H, Howell RT, Cope C. Curtis H, et al. Among authors: howell rt. J Med Genet. 1986 Oct;23(5):478-80. doi: 10.1136/jmg.23.5.478. J Med Genet. 1986. PMID: 3783629 Free PMC article.
A new apparently folate sensitive fragile site, 5q35.
Howell RT, McDermott A, Evans JL. Howell RT, et al. J Med Genet. 1990 Aug;27(8):527-8. doi: 10.1136/jmg.27.8.527. J Med Genet. 1990. PMID: 2213847 Free PMC article. No abstract available.
56 results