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American Journal of Medical Genetics|February 1, 1991
Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosisM S Krawczun, E C Jenkins, C J Duncan, et al.American Journal of Medical Genetics|May 1, 1988
Aneuploidy and the fragile X syndromeM S Watson, W R Breg, D Pauls, et al.Human Genetics|March 1, 1988
Multilocus analysis of the fragile X syndromeW T Brown, A Gross, C Chan, et al.Neurology. Genetics|March 12, 2021
Biallelic Variants in the COLGALT1 Gene Causes Severe Congenital Porencephaly: A Case ReportMariel W A Teunissen, Erik-Jan Kamsteeg, Suzanne C E H Sallevelt, et al.American Journal of Medical Genetics|May 20, 1999
FRAXAC1 and DXS548 polymorphisms in the Chinese populationP M Poon, C P Pang, Q L Chen, et al.American Journal of Ophthalmology|April 26, 2025
Two novel extended depth-of-focus intraocular lenses targeted for mini-monovision: A prospective randomized controlled trialJoukje C Wanten, Noël J C Bauer, Tos T J M Berendschot, et al.Human Genetics|April 1, 1987
Further evidence for genetic heterogeneity in the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.American Journal of Medical Genetics|August 9, 1996
Tissue differences in fragile X mosaics: mosaicism in blood cells may differ greatly from skinC S Dobkin, S L Nolin, I Cohen, et al.American Journal of Medical Genetics|January 1, 1986
Mouse chromosome fragilityM M Sanz, E C Jenkins, W T Brown, et al.Journal of Cataract and Refractive Surgery|January 24, 2025
Dissatisfaction after implantation of EDOF intraocular lensesJoukje C Wanten, Noël J C Bauer, Tos T J M Berendschot, et al.Pageof 23