Paternal transmission of congenital myotonic dystrophy.

Por Bergoffen, J, Kant, J, Sladky, J, McDonald-McGinn, D, Zackai, E H, Fischbeck, K H
Publicado em 1994

Linkage localization of X-linked Charcot-Marie-Tooth disease.

Por Bergoffen, J, Trofatter, J, Pericak-Vance, M A, Haines, J L, Chance, P F, Fischbeck, K H
Publicado em 1993

X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.

Por Cochrane, S, Bergoffen, J, Fairweather, N D, Müller, E, Mostacciuolo, M L, Monaco, A P, Fischbeck, K H, Haites, N E
Publicado em 1994

Molecular study of three cases of odontohypophosphatasia resulting from heterozygosity for mutations in the tissue non-specific alkaline phosphatase gene

Por Herasse, M, Spentchian, M, Taillandier, A, Keppler-Noreuil, K, Fliorito, A, Bergoffen, J, Wallerstein, R, Muti, C, Simon-Bouy, B, Mornet, E
Publicado em 2003