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Clinical Genetics|December 1, 1980
Ring chromosome 15 in a male adult with radial defects. Evaluation of the phenotypeP Meinecke, T Koske-WestphalAmerican Journal of Medical Genetics|June 14, 1996
Bilateral porencephaly, cerebellar hypoplasia, and internal malformations: two siblings representing a probably new autosomal recessive entityC G Bönnemann, P MeineckeJournal of Medical Genetics|April 1, 1990
Fetal brain disruption sequence: a milder variantC G Bönnemann, P MeineckeClinical Dysmorphology|July 1, 1992
Campomelic dysplasia without overt campomeliaU Friedrich, E Schaefer, P MeineckeGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Potter sequence due to renal aplasia and postaxial hexadactyly. A distinct entity?P Meinecke, W Ziegenrücker, A PetersClinical Dysmorphology|October 1, 1995
Fryns syndrome: two further cases without lateral diaphragmatic defectsO Bartsch, P Meinecke, G KaminMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1987
[Cerebro-costo-mandibular syndrome without cerebral involvement in a 4-year-old boy]P Meinecke, G Wolff, E SchaeferClinical Genetics|August 1, 1985
EEC syndrome without ectrodactyly? Report of 8 casesW Küster, F Majewski, P MeineckeAmerican Journal of Medical Genetics|May 3, 1996
Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?E Majewski, T Goecke, P MeineckeEuropean Journal of Pediatrics|July 1, 1991
Further delineation of the ichthyosis follicularis, atrichia, and photophobia syndromeH Hamm, P Meinecke, H TraupePageof 14