H.‐J. Lüdecke

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

H.‐J. Lüdecke, Jörg Schaper, Peter Meinecke et al. · The American Journal of Human Genetics · 2001 · 234 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +4

The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletions

Judith Nardmann, Lisbeth Tranebjærg, Bernhard Horsthemke et al. · Human Genetics · 1997 · 91 citations

Developmental Anomaly, Genetics, Pediatrics +2

Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome.

H.‐J. Lüdecke, Colin A. Johnson, M.J. Wagner et al. · PubMed · 1991 · 80 citations

Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype

Nuria C. Bramswig, Oana Caluseriu, H.‐J. Lüdecke et al. · Human Genetics · 2017 · 74 citations

Genetic Disorder, Medicine, Genetics +8

Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism

Nuria C. Bramswig, H.‐J. Lüdecke, Maria Pettersson et al. · Human Genetics · 2016 · 62 citations

Neurodevelopmental Disorders, Intellectual Impairment, Developmental Disability +12