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Clinical Genetics|May 1, 2008
Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotypeL Avrahami, S Maas, M Pasmanik-Chor, et al.
The Israel Medical Association Journal : IMAJ|September 9, 2000
Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterizationT C Falik-Zaccai, E Shachak, D Abeliovitch, et al.
Genomics|September 1, 1990
Serum amyloid A and P protein genes in familial Mediterranean feverM Shohat, T Shohat, J I Rotter, et al.
Scandinavian Journal of Immunology|May 1, 1991
Regulation of human interleukin-2 and interferon-gamma gene expression by suppressor T lymphocytesM Ketzinel, S Efrat, D Sayar, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 31, 2017
Cut-off value of nuchal translucency as indication for chromosomal microarray analysisI Maya, S Yacobson, S Kahana, et al.
American Journal of Human Genetics|July 10, 2001
Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in IsraelH Toledano-Alhadef, L Basel-Vanagaite, N Magal, et al.
Clinical Genetics|November 1, 1990
Genetic marker family studies in familial Mediterranean fever (FMF) in ArmeniansT Shohat, M Shohat, G M Petersen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafnessY Bykhovskaya, H Yang, K Taylor, et al.
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