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Journal of Medical Genetics|March 1, 1989
Limb anomalies in the CHARGE associationP Meinecke, A Polke, P SchmiegelowAmerican Journal of Medical Genetics|October 1, 1990
Agnathia, holoprosencephaly, and situs inversus: a third reportP Meinecke, B Padberg, R LaasKlinische Padiatrie|January 1, 1983
[Congenital contractural arachnodactyly (CCA syndrome)--an autosomal dominant hereditary connective tissue disease]P Meinecke, E Schaefer, E PassargeClinical Dysmorphology|July 1, 1992
Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritanceA Artlich, E Schwinger, P MeineckeMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|February 1, 1990
[Brachmann-de Lange syndrome in 16 of our patients]R Pankau, W Johannson, P MeineckeGeburtshilfe Und Frauenheilkunde|December 1, 1976
[Acute occlusion of the arterial blood supply of the right arm in a newborn following entanglement of the umbilical cord (author's transl)]H Muth, R EngelbrechtClinical Performance and Quality Health Care|March 8, 1997
DIABCARD a smart card for patients with chronic diseasesR Engelbrecht, C HildebrandStudies in Health Technology and Informatics|April 5, 2000
Telemedicine and diabetesR Engelbrecht, C HildebrandClinical Dysmorphology|January 1, 1992
Microgastria-hypoplastic upper limb association: a severe expression including microphthalmia, single nostril and arhinencephalyP Meinecke, C G Bönnemann, R LaasJournal of Medical Genetics|January 1, 1991
Balanced t(6;8)(6p8p;6q8q) and the CHARGE associationJ A Hurst, P Meinecke, M BaraitserPageof 14