A Case of Compound Mutations in the MYBPC3 Gene Associated with Biventricular Hypertrophy and Neonatal Death

Publisher： Karger

E-ISSN： 1661-7819|102|4|254-258

ISSN： 1661-7800

Source： Neonatology, Vol.102, Iss.4, 2012-08, pp. : 254-258

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

Rapid Detection of Common Mutations of the FGFR3 Gene Causing Thanatophoric Dysplasia Type I: Two Case Reports

By Yang Yu   Liu Ying-Na   Li Dong-Zhi  

Fetal and Pediatric Pathology, Vol. 31, Iss. 3, 2012-05 ,pp. : 128-133

Informa Healthcare

Access to resources Recommend Favorite

SUDDEN INFANT DEATH SYNDROME AND ACTIVATING GNAS1 GENE MUTATIONS

By Román Rossana   López Patricia   Johnson María Cecilia   Boric María Angélica   Gallo Miriam   Ponce Carolina   Vargas Sergio   Codner Ethel   Cassorla Fernando  

Fetal and Pediatric Pathology, Vol. 26, Iss. 4, 2007-07 ,pp. : 199-205

Informa Healthcare

Access to resources Recommend Favorite

Syndromes Caused by the Mutations in GLI3 Gene

By  

Current Pediatric Reviews, Vol. 6, Iss. 4, 2010-11 ,pp. : 219-225

Bentham Science Publishers

Access to resources Recommend Favorite

Case of Large Placental Chorioangioma Associated with Diffuse Neonatal Hemangiomatosis

By Bakaris Sevgi  

Pediatric and Developmental Pathology, Vol. 7, Iss. 3, 2004-06 ,pp. : 258-261

Springer Publishing Company

Access to resources Recommend Favorite

A Novel and a Previously Described Compound Heterozygous PKLR Gene Mutations Causing Pyruvate Kinase Deficiency in a Chinese Child

By Li Huimin   Gu Ping   Yao Ru-en   Wang Jian   Fu Qihua   Wang Jing  

Fetal and Pediatric Pathology, Vol. 33, Iss. 3, 2014-06 ,pp. : 182-190

Informa Healthcare

Access to resources Recommend Favorite