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[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|December 26, 2019
[Correct clinical diagnosis and treatment of dry eye]J Hong
American Journal of Human Genetics|December 1, 1991
Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizationsR Feil, P Aubourg, J Mosser, et al.
American Journal of Human Genetics|December 5, 1998
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutationsS Jacquot, K Merienne, D De Cesare, et al.
Infection Control and Hospital Epidemiology|April 1, 1992
A cluster of vancomycin-resistant Enterococcus faecium in an intensive care unitL V Karanfil, M Murphy, A Josephson, et al.
Human Genetics|May 1, 1994
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpointM Chery, V Biancalana, C Philippe, et al.
Folia Biologica|January 1, 1992
Autoimmunity: from physiology to pathology. Natural antibodies, mucosal immunity and development of B cell repertoireH Tlaskalová-Hogenová, L Mandel, R Stĕpánková, et al.
Genomics|April 1, 1988
Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouseL C Amar, L Dandolo, A Hanauer, et al.
AJR. American Journal of Roentgenology|September 1, 1991
Parotid enlargement in children seropositive for human immunodeficiency virus: imaging findingsN Soberman, J C Leonidas, W E Berdon, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture systemO M Dorchies, J Laporte, S Wagner, et al.
American Journal of Human Genetics|April 16, 1998
Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of familiesL Cavalier, K Ouahchi, H J Kayden, et al.
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