De novo 4q duplication/deletion in a fetus with a congenital heart defect

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 8, 2015-08 ,pp. : 1932-1936

John Wiley & Sons Inc

Access to resources Recommend Favorite

De novo 9q gain in an infant with tetralogy of Fallot with absent pulmonary valve: Patient report and review of congenital heart disease in 9q duplication syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 2966-2974

John Wiley & Sons Inc

Access to resources Recommend Favorite

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

By  

Molecular Syndromology, Vol. 6, Iss. 1, 2015-01 ,pp. : 32-38

Karger

Access to resources Recommend Favorite

Identification of familial and de novo microduplications of 22q11.21q11.23 distal to the 22q11.21 microdeletion syndrome region

By Coppinger Justine   McDonald-McGinn Donna   Zackai Elaine   Shane Kate   Atkin Joan F.   Asamoah Alexander   Leland Robert   Weaver David D.   Lansky-Shafer Susan   Schmidt Karen   Feldman Heidi   Cohen William   Phalin Judy   Powell Berkley   Ballif Blake C.   Theisen Aaron   Geiger Elizabeth   Haldeman-Englert Chad   Shaikh Tamim H.   Saitta Sulagna   Bejjani Bassem A.   Shaffer Lisa G.  

Human Molecular Genetics, Vol. 18, Iss. 8, 2009-04 ,pp. : 1377-1383

Oxford University Press

Access to resources Recommend Favorite

The behavioral characteristics of Sotos syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 2945-2956

John Wiley & Sons Inc

Access to resources Recommend Favorite