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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1988
[Abnormalities-retardation syndrome caused by incomplete triploidy]P Meinecke, R EngelbrechtEuropean Journal of Pediatrics|October 1, 1983
The Weaver syndrome in a girlP Meinecke, E Schaefer, R EngelbrechtMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1986
[Coffin-Siris syndrome in a 5-year-old girl]P Meinecke, R Engelbrecht, E SchaeferGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second familyP MeineckeKlinische Padiatrie|March 1, 1982
[Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)]P MeineckeDeutsche Medizinische Wochenschrift (1946)|October 20, 1978
[Syndrome of symphalangism and stapes fixation: an autosomal dominant hereditary disease (author's transl)]P Meinecke, E PassargeJournal of Medical Genetics|November 1, 1991
Microcephalic osteodysplastic primordial dwarfism type I/III in sibsP Meinecke, E PassargeJournal of Medical Genetics|June 1, 1989
Frontonasal dysplasia, congenital heart defect, and short stature: a further observationP Meinecke, W BlunckJournal of Medical Genetics|March 1, 1990
Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomaliesP Meinecke, H HayekDer Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 1, 1993
[CHILD syndrome. Case report of a rare genetic dermatosis]C Peter, P MeineckePageof 14