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

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|12|2966-2974

ISSN： 1552-4825

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

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 5q35.5 duplication with clinical presentation of Sotos syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2501-2507

John Wiley & Sons Inc

Access to resources Recommend Favorite

Familial TAB2 microdeletion and congenital heart defects including unusual valve dysplasia and tetralogy of fallot

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2702-2706

John Wiley & Sons Inc

Access to resources Recommend Favorite

Duplication of 10q22.3–q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 3174-3179

John Wiley & Sons Inc

Access to resources Recommend Favorite

Paternal uniparental disomy chromosome 14‐like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG‐ and the MEG3‐DMRs: Patient report and genotype–phenotype correlation

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 3130-3138

John Wiley & Sons Inc

Access to resources Recommend Favorite