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2002 1
2003 3
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2008 2
2009 1
2020 1
2021 1
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Page 1
Phaeochromocytoma in children.
Armstrong R, Sridhar M, Greenhalgh KL, Howell L, Jones C, Landes C, McPartland JL, Moores C, Losty PD, Didi M. Armstrong R, et al. Among authors: greenhalgh kl. Arch Dis Child. 2008 Oct;93(10):899-904. doi: 10.1136/adc.2008.139121. Epub 2008 May 22. Arch Dis Child. 2008. PMID: 18499773 Review.
Siblings with Bohring-Opitz syndrome.
Greenhalgh KL, Newbury-Ecob RA, Lunt PW, Dolling CL, Hargreaves H, Smithson SF. Greenhalgh KL, et al. Clin Dysmorphol. 2003 Jan;12(1):15-9. doi: 10.1097/00019605-200301000-00003. Clin Dysmorphol. 2003. PMID: 12514360
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. 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.
Novel corneal features in two males with incontinentia pigmenti.
Mayer EJ, Shuttleworth GN, Greenhalgh KL, Sansom JE, Grey RH, Kenwrick S. Mayer EJ, et al. Among authors: greenhalgh kl. Br J Ophthalmol. 2003 May;87(5):554-6. doi: 10.1136/bjo.87.5.554. Br J Ophthalmol. 2003. PMID: 12714390 Free PMC article.