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Clinical Genetics|February 1, 1984
A new psychomotor retardation syndrome with peculiar facies and marfanoid habitusR Fragoso, J M CantúClinical Genetics|March 1, 1984
Alpha-mannosidosis: analysis of urinary oligosaccharides with high performance liquid chromatography and diagnosis of a case with unusually mild presentationT G Warner, A K Mock, W L Nyhan, et al.Clinical Genetics|March 1, 1984
Problems of detecting mosaicism in skin. A case of trisomy 8 mosaicism illustrating the advantages of in situ tissue cultureS E Procter, J L Watt, D J Lloyd, et al.Clinical Genetics|March 1, 1984
Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical pictureH F de France, F A Beemer, R C Senders, et al.Clinical Genetics|July 1, 1983
Do the MN and Jk systems influence environmental variability in serum lipid levels?N G Martin, D M Rowell, J B WhitfieldClinical Genetics|June 1, 1984
Five generations of t(4;8)(q35;q13) leading to a case of partial 8q trisomy with consideration of potential pregnancy outcomes from translocation carriersR S Young, K L Hansen, G S KhodrClinical Genetics|January 3, 2026
Unusual Disease-Progression in Two Siblings With Xeroderma Pigmentosum Group GElena Botta, Heather Fawcett, Donata Orioli, et al.Clinical Genetics|February 1, 1979
Monoamine oxidase and catechol-o-methyltransferase activity in cultured fibroblasts from patients with maple syrup urine disease, Lesch-Nyhan syndrome and healthy controlsS Singh, I Willers, E M Kluss, et al.Clinical Genetics|February 1, 1979
Counseling for dominant traits: a correction for the ascertainment bias due to referral for analysisK Gladstien, M A SpenceClinical Genetics|February 1, 1979
Melkersson-Rosenthal's syndrome in four generationsC Lygidakis, C Tsakanikas, A Ilias, et al.Pageof 718