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Pediatric Research|May 1, 1980
A new variant of galactosemia: galactose-1-phosphate uridylytransferase sensitive to product inhibition by glucose 1-phosphateA Lang, H Groebe, B Hellkuhl, et al.Annales De Genetique|January 1, 1984
Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/splitfoot malformationR A PfeifferMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1987
[Genetic counseling and prenatal diagnosis: from where, to where? A personal commentary]R A PfeifferRofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|August 1, 1976
[Acromesomelic dwarfism (author's transl)A1]R A PfeifferGeburtshilfe Und Frauenheilkunde|August 1, 1983
[Prenatal cytogenetics. Indications--organization--problems]R A PfeifferCytogenetics and Cell Genetics|January 1, 1980
Observations in a case of an X/Y translocation, t(X;Y)(p22;q11), in a mother and sonR A PfeifferClinical Genetics|August 1, 1980
Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22)R A PfeifferHuman Heredity|January 1, 1984
Evidence that activities of coagulation factors VII and X are linked to chromosome 13 (q34)R Ott, R A PfeifferAnnales De Genetique|January 1, 1993
Tandem duplication 11q23-ter in the dysmorphic child of a retarded mother mosaic for the same anomaly with no apparent abnormalitiesR A Pfeiffer, C SchützJournal of Neurology|July 20, 1977
[Hypoplasia ponto-neocerebellaris (author's transl)]J Peiffer, R A PfeifferPageof 13