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

ISSN： 1551-3815

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

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

Related content

COMMON ARTERIAL TRUNK WITH THANATOPHORIC DYSPLASIA: A UNIQUE CASE

By McBrien Angela Sands Andrew Paterson Annie Tharmaratnam Suresh Thornton Claire

Fetal and Pediatric Pathology, Vol. 27, Iss. 6, 2008-04 ,pp. : 259-263

Informa Healthcare

Access to resources Recommend Favorite

THANATOPHORIC DYSPLASIA TYPE I ASSOCIATED WITH INCREASED NUCHAL TRANSLUCENCY IN THE FIRST TRIMESTER: Early Prenatal Diagnosis Using Combined Ultrasonography and Molecular Biology

By Tonni Gabriele Azzoni Daniela Ventura Alessandro Ferrari Bruno Felice Claudio De Baldi Maurizia

Fetal and Pediatric Pathology, Vol. 29, Iss. 5, 2010-08 ,pp. : 314-322

Informa Healthcare

Access to resources Recommend Favorite

Dentinal Dysplasia Type I: Report of an Atypical Case in the Primary Dentition

By Vieira Alexandra Rezende Modesto Adriana Cabral Márcia Grillo

Journal of Dentistry for Children, Vol. 65, Iss. 2, 1998-03 ,pp. : 141-144

American Academy of Pediatric Dentistry

Access to resources Recommend Favorite

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

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

Karger

Access to resources Recommend Favorite

Syndromes Caused by the Mutations in GLI3 Gene

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

Bentham Science Publishers

Access to resources Recommend Favorite