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American Journal of Medical Genetics|September 1, 1990
A sibship with Roberts/SC phocomelia syndromeM Holmes-Siedle, A Seres-Santamaria, M Crocker, et al.
American Journal of Ophthalmology|February 15, 1985
Oculocerebrocutaneous syndromeR D Wilson, L Traverse, J G Hall, et al.
Teratology|February 1, 1986
Studies of human achondroplasia: oxidative metabolism in tissue culture cellsB Mackler, R Grace, K A Davis, et al.
Clinical Genetics|January 1, 1979
No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45, XO Turner syndromeJ L Burns, J G Hall, E Powers, et al.
Human Genetics|August 31, 1977
Small structural changes of chromosome 8. Two cases with evidence for deletionC Beighle, L E Karp, J W Hanson, et al.
Archives of Neurology|May 1, 1989
Joubert's syndrome associated with congenital ocular fibrosis and histidinemiaR E Appleton, D Chitayat, J E Jan, et al.
Clinical Genetics|April 1, 1985
Chromosomal abnormalities associated with congenital contractures (arthrogryposis)S D Reed, J G Hall, V M Riccardi, et al.
Clinical Genetics|February 1, 1978
Amniotic fluid cell mosaicism for presumptive trisomy 20M L Rodriguez, D Luthy, J G Hall, et al.
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