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au.\*:("SEBOLD, Courtney")

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Perception of disease Severity in adolescents diagnosed with neurofibromatosis type 1SEBOLD, Courtney Drake; LOVELL, Anne; HOPKIN, Robert et al.Journal of adolescent health. 2004, Vol 35, Num 4, pp 297-302, issn 1054-139X, 6 p.Article

The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletionsHASI, Minire; SOILEAU, Bridgette; SEBOLD, Courtney et al.Human genetics. 2011, Vol 130, Num 6, pp 777-787, issn 0340-6717, 11 p.Article

Narrowing Critical Regions and Determining Penetrance for Selected 18q- PhenotypesCODY, Jannine D; HEARD, Patricia L; SCHAUB, Rebecca L et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1421-1430, issn 1552-4825, 10 p.Article

Founder and Recurrent CDH1 mutations in families with Hereditary diffuse gastric Cancer. EditorialKAURAH, Pardeep; MACMILLAN, Andrée; NIKKEL, Sarah et al.JAMA, the journal of the American Medical Association. 2007, Vol 297, Num 21, issn 0098-7484, 2360-2411 [15 p.]Article

Tetrasomy 18p: Report of the Molecular and Clinical Findings of 43 IndividualsSEBOLD, Courtney; ROEDER, Elizabeth; O'DONNELL, Louise et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 9, pp 2164-2172, issn 1552-4825, 9 p.Article

Genetic determinants of autism in individuals with deletions of 18qO'DONNELL, Louise; SOILEAU, Bridgette; HEARD, Patricia et al.Human genetics. 2010, Vol 128, Num 2, pp 155-164, issn 0340-6717, 10 p.Article

High Resolution Genomic Analysis of 18q― Using Oligo-Microarra Comparative Genomic Hybridization (aCGH)HEARD, Patricia L; CARTER, Erika M; CRANDALL, Analisa C et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1431-1437, issn 1552-4825, 7 p.Article

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