H.‐D. Rott

Kartagener's syndrome and the syndrome of immotile cilia

H.‐D. Rott · Human Genetics · 1979 · 110 citations

Clinical Disorders, Genetic Disorder, Pathology +2

A study of ten small supernumerary (marker) chromosomes identified by fluorescence <i>in situ</i> hybridization (FISH)

Anita Rauch, R. A. Pfeiffer, Udo Trautmann et al. · Clinical Genetics · 1992 · 83 citations

Additional Marker Idic, Cytogenetics, Genetics +20

A serologic study of organisms possibly associated with pertussis-like coughing

Carl Heinz Wirsing von König, H.‐D. Rott, H. Bogaerts et al. · The Pediatric Infectious Disease Journal · 1998 · 64 citations

A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus

Raimund Fahsold, H.‐D. Rott, Peter Lorenz · Human Genetics · 1991 · 53 citations

Mendelian Disorder, Genetic Disorder, Genetics +9

X-linked ocular albinism

Gabriele E. Lang, H.‐D. Rott, R. A. Pfeiffer · Ophthalmic Paediatrics and Genetics · 1990 · 49 citations