Oesophagus

Citations 11-16 of 16 total displayed.

Electronic letters
Laugier-Hunziker syndrome: an important differential diagnosis for Peutz-Jeghers syndrome

A K Lampe, P J Hampton, K Woodford-Richens, I Tomlinson, C M Lawrence, F S Douglas
J. Med. Genet. 2003; 40: e77. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER association

ROBERTA CINTI, MANUELA PRIOLO, MARGHERITA LERONE, GIORGIO GIMELLI, MARCO SERI, MARGHERITA SILENGO, ROBERTO RAVAZZOLO
J. Med. Genet. 2001; 38: e6. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Deletion (2)(p14p15) in a child with severe neurodevelopmental delay

ISAM M AMIR, KHALIL I AL-TAWIL, MUNEEF M AL-HATHAL
J. Med. Genet. 2000; 37: e21. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
A family with hereditary port wine stain

JONATHAN N BERG, A A QUABA, A GEORGANTOPOULOU, MARY E M PORTEOUS
J. Med. Genet. 2000; 37: e12. [Extract] [Full text] [PDF] [Request Permissions]  

Short reports
De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings

Simone Schuffenhauer, Hans-Jürgen Leifheit, Peter Lichtner, Heiko Peters, Jan Murken, P Emmerich
J. Med. Genet. 1999; 36: 233-236. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Microdeletion 22q11 and oesophageal atresia

Maria Cristina Digilio, Bruno Marino, Pietro Bagolan, Aldo Giannotti, Bruno Dallapiccola
J. Med. Genet. 1999; 36: 137-139. [Abstract] [Full text] [PDF] [Request Permissions]