J. Herrmann

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Suzanne B. Cassidy, Li‐Wen Lai, Robert P. Erickson et al. · PubMed · 1992 · 179 citations

The translocation t(1;22)(p13;q13) is a nonrandom marker specifically associated with acute megakaryocytic leukemia in young children

Thomas Lion, OA Haas, Jochen Harbott et al. · Blood · 1992 · 116 citations · Full text

The Stickler syndrome (hereditary arthroophthalmopathy).

J. Herrmann, Thomas D. France, Jürgen W. Spranger et al. · Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) · 1975 · 113 citations

Ocular Disease, Ophthalmology, Degenerative Diseases +4

Poland syndrome in British Columbia: Incidence and reproductive experience of affected persons

Barbara McGillivray, R. Brian Lowry, J. Herrmann · American Journal of Medical Genetics · 1977 · 110 citations

Cutis marmorata telangiectatica congenita

Barbara H. Way, J. Herrmann, Enid F. Gilbert et al. · Journal of Cutaneous Pathology · 1974 · 108 citations

Cutis Marmorata, Venous Disease, Secondary Thrombosis +12