E. Stéphan

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3

A. Mégarbané, J. Loiselet, V. Delague, 2000, European Journal of Human Genetics.

Hereditary bundle branch system defect. A new genetic entity?

E. Stéphan, 1979, American heart journal.

Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorder.

A. Mégarbané, J. Loiselet, P. Bouvagnet, 1999, American journal of medical genetics.

Hereditary bundle branch system defect: survey of a family with four affected generations.

E. Stéphan, 1978, American heart journal.

Ring-chromosom 18

J. Kunze, E. Stéphan, M. Tolksdorf, 1972, Humangenetik.

[Ring chromosome 18. 18p-/18q- -deletion-syndrome].

J. Kunze, E. Stéphan, M. Tolksdorf, 1972, Humangenetik.

An isolated cardiac conduction disease maps to chromosome 19q.

J. Weissenbach, J. Loiselet, J. Demaille, 1995, Circulation research.

Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristics.

P. Bouvagnet, A de Meeus, P Bouvagnet, 1997, American heart journal.

[Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case].

A. Mégarbané, J. Loiselet, P. Bouvagnet, 2000, Archives des maladies du coeur et des vaisseaux.