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Alan Shanske

Showing results (1-10 of 20) with videos related to

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The New York State Dental Journal|August 24, 2006
Craniofacial characteristics evidenced in Bartsocas-Papas syndrome from birth to five years. Case reportAnthony L Maganzini, Andrea Rios, Alan Shanske
The Journal of Pediatrics|October 18, 2005
All shook up by SHOX deficiencyGudrun A Rappold, Alan Shanske, Paul Saenger
American Journal of Medical Genetics. Part A|May 17, 2007
Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndromePooja Gidwani, Eric Segal, Alan Shanske, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|April 17, 2008
Retinoic acid-induced inner ear teratogenesis caused by defective Fgf3/Fgf10-dependent Dlx5 signalingWei Liu, Giovanni Levi, Alan Shanske, et al.
American Journal of Medical Genetics. Part A|May 12, 2006
T-genes and limb bud developmentMary King, Jelena S Arnold, Alan Shanske, et al.
Growth Factors (Chur, Switzerland)|November 11, 2008
Coordinated molecular control of otic capsule differentiation: functional role of Wnt5a signaling and opposition by sfrp3 activityWei Liu, Lijun Li, Geming Li, et al.
Archives of Pediatrics & Adolescent Medicine|November 7, 2002
A recurring FBN1 gene mutation in neonatal Marfan syndromeAmanda M Jacobs, Ivanka Toudjarska, Andrew Racine, et al.
American Journal of Medical Genetics. Part A|March 16, 2007
Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairmentJoy Samanich, Christina Lowes, Robert Burk, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2008
Genetic evaluation of American minority pediatric cochlear implant recipientsTova C Fischer, Joy Samanich, Bernice E Morrow, et al.
Archives of Dermatology|January 20, 2010
Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected familyMichelle Yadegari, Michael P Whyte, Steven Mumm, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
The New York State Dental Journal|August 24, 2006
Craniofacial characteristics evidenced in Bartsocas-Papas syndrome from birth to five years. Case reportAnthony L Maganzini, Andrea Rios, Alan Shanske
The Journal of Pediatrics|October 18, 2005
All shook up by SHOX deficiencyGudrun A Rappold, Alan Shanske, Paul Saenger
American Journal of Medical Genetics. Part A|May 17, 2007
Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndromePooja Gidwani, Eric Segal, Alan Shanske, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|April 17, 2008
Retinoic acid-induced inner ear teratogenesis caused by defective Fgf3/Fgf10-dependent Dlx5 signalingWei Liu, Giovanni Levi, Alan Shanske, et al.
American Journal of Medical Genetics. Part A|May 12, 2006
T-genes and limb bud developmentMary King, Jelena S Arnold, Alan Shanske, et al.
Growth Factors (Chur, Switzerland)|November 11, 2008
Coordinated molecular control of otic capsule differentiation: functional role of Wnt5a signaling and opposition by sfrp3 activityWei Liu, Lijun Li, Geming Li, et al.
Archives of Pediatrics & Adolescent Medicine|November 7, 2002
A recurring FBN1 gene mutation in neonatal Marfan syndromeAmanda M Jacobs, Ivanka Toudjarska, Andrew Racine, et al.
American Journal of Medical Genetics. Part A|March 16, 2007
Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairmentJoy Samanich, Christina Lowes, Robert Burk, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2008
Genetic evaluation of American minority pediatric cochlear implant recipientsTova C Fischer, Joy Samanich, Bernice E Morrow, et al.
Archives of Dermatology|January 20, 2010
Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected familyMichelle Yadegari, Michael P Whyte, Steven Mumm, et al.
Pageof 2