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https://www.ias.ac.in/article/fulltext/jgen/092/01/0097-0101

holoprosencephaly; Currarino syndrome; 7q36 deletion; SHH gene mutation.

Francesca Lami¹ Diana Carli² Paola Ferrari¹ Monica Marini³ Viola Alesi⁴ Lorenzo Iughetti¹ Antonio Percesepe²

1. Pediatrics Unit, Department of Mother and Child, University of Modena, Via del Pozzo 71, 41124 Modena, Italy
2. Medical Genetics Units, Department of Mother and Child, University of Modena, Via del Pozzo 71, 41124 Modena, Italy
3. Laboratory of Molecular Genetics, Department of Pediatrics and CEBR, University of Genova, Largo G. Gaslini 5, 16147 Genova, Italy
4. Medical Genetics Unit, S. Pietro Fatebenefratelli Hospital, Via Cassia 600, 00189 Rome, Italy

Published

April 2013

Manuscript received

26 July 2012

Manuscript revised

5 November 2012

Accepted

16 November 2012

Early published

2 April 2013