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Page 1
Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors.
J Genet Couns. 2007 Aug;16(4):387-407. doi: 10.1007/s10897-007-9101-8. Epub 2007 Jul 17.
J Genet Couns. 2007.
PMID: 17636453
Free PMC article.
Review.
Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).
Sebold CD, Romie S, Szymanska J, Torres-Martinez W, Thurston V, Muesing C, Vance GH.
Sebold CD, et al.
Am J Med Genet A. 2005 Apr 1;134A(1):80-3. doi: 10.1002/ajmg.a.30463.
Am J Med Genet A. 2005.
PMID: 15690398
Review.
Item in Clipboard
Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele.
Sebold CD, Melvin EC, Siegel D, Mehltretter L, Enterline DS, Nye JS, Kessler J, Bassuk A, Speer MC, George TM; NTD Collaborative Group.
Sebold CD, et al.
Genet Med. 2005 Jan;7(1):64-7. doi: 10.1097/01.gim.0000151158.09278.2b.
Genet Med. 2005.
PMID: 15654231
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Perception of disease severity in adolescents diagnosed with neurofibromatosis type 1.
Sebold CD, Lovell A, Hopkin R, Noll R, Schorry E.
Sebold CD, et al.
J Adolesc Health. 2004 Oct;35(4):297-302. doi: 10.1016/j.jadohealth.2003.10.003.
J Adolesc Health. 2004.
PMID: 15450543
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