Moshe Frydman

Multiple supernumerary teeth (MSNT) and Ehlers-Danlos syndrome (EDS): a case report.

M. Frydman, G. Barkai, Y. Melamed, 1994, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Wilson's disease in Israel: a genetic and epidemiological study

L. Cavalli-Sforza, A. Bowcock, B. Bonné-Tamir, 1990, Annals of human genetics.

Familial lipoid adrenal hyperplasia: genetic marker data and an approach to prenatal diagnosis.

B. Bonné-Tamir, M. Frydman, A. Kauschansky, 1986, American journal of medical genetics.

Eight closely linked loci place the Wilson disease locus within 13q14-q21.

A. Bowcock, L. Farrer, H. Scheffer, 1988, American journal of human genetics.

Familial syndromic esophageal atresia maps to 2p23-p24.

J. Celli, H. Bokhoven, R. Hennekam, 2000, American journal of human genetics.

Alpers progressive infantile neuronal poliodystrophy: an acute neonatal form with findings of the fetal akinesia syndrome.

L. D. de Vries, L. Sirota, M. Frydman, 1993, American journal of medical genetics.

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

K. Avraham, M. Frydman, A. Orr-Urtreger, 1999, Human Genetics.