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Genetic 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 MeineckeGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Intrauterine growth retardation, mild frontonasal dysplasia, phocomelic upper limbs with absent thumbs and a variety of internal malformations including choanal atresia, congenital heart defects, polysplenia, absent gall bladder as well as genitourinary anomalies. A possibly "new" MCA syndrome?P Meinecke, M PeperAmerican Journal of Medical Genetics|October 1, 1987
A specific syndrome due to deletion of the distal long arm of chromosome 1P Meinecke, D VögtelMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1991
[FG syndrome in 2 half brothers]C Wieg, P MeineckePageof 20