Publications by authors named "David B Flannery"

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Challenges and opportunities for effective delivery of clinical genetic services in the U.S. healthcare system.
David B Flannery

Curr Opin Pediatr· December 2018

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Complete monosomy 21 confirmed by FISH and array-CGH.
Anita S Kulharya, Vijay S Tonk, Carolyn Lovell, David B Flannery

Am J Med Genet A· April 2012

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Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
Paweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, Srirangan Sampath, Samarth S Bhatt, David B Flannery

Hum Mutat· January 2012

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Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.
Anita S Kulharya, David B Flannery, Karen Norris, Carolyn Lovell, Brynn Levy

Am J Med Genet A· September 2008

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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
Jennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, Emma Elson, Joyce T Turner, David B Flannery

Am J Hum Genet· April 2005

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Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
Anita S Kulharya, Carolyn Mills Lovell, David B Flannery

Am J Med Genet· December 2002

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