A. Heimler

发表

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.

J. Opitz, E. Lieber, A. Heimler, 1986, American journal of medical genetics.

An Oral History of the National Society of Genetic Counselors

A. Heimler, 1997, Journal of Genetic Counseling.

Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6

S. Ferdinandusse, H. Waterham, W. Newman, 2015, American journal of human genetics.

Sensorineural hearing loss, enamel hypoplasia, and nail abnormalities in sibs.

J. Hershey, J. Fox, A. Heimler, 1991, American journal of medical genetics.

Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family.

A. Rosenthal, A. Heimler, E. Friedman, 1978, Journal of medical genetics.

Testicular feminisation and inguinal hernia.

E. Pergament, A. Heimler, P. Shah, 1973, Lancet.

Autosomal dominant transmission of ureteral triplication and bilateral amastia.

W. Brock, M. Rich, L. Waber, 1987, The Journal of urology.

An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family.

J. Sciubba, E. Lieber, S. Kamen, 1985, Oral surgery, oral medicine, and oral pathology.

Letters to the editor

S. Hodge, A. Heimler, 1996, Journal of Genetic Counseling.

Huntington disease: A case study describing the complexities and nuances of predictive testing of monozygotic twins

A. Zanko, A. Heimler, 1995, Journal of Genetic Counseling.

Genetic aspects of shell teeth: report of case.

S. Kamen, A. Heimler, D. Goodman, 1980, ASDC journal of dentistry for children.

Twoautosomal dominant disorders segregating inafamily1

A. Heimler, E. Friedman, 1978 .