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Genomics|January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndromeG Palmieri, V Capra, G Romano, et al.
Optics Express|February 7, 2018
Graded SiGe waveguides with broadband low-loss propagation in the mid infraredJ M Ramirez, Q Liu, V Vakarin, et al.
Human Molecular Genetics|December 15, 2000
Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1M d'Addio, A Pizzigoni, M T Bassi, et al.
Genomics|January 1, 1989
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levelsA Ballabio, R Carrozzo, G Parenti, et al.
Optics Express|April 7, 2017
Ge-rich graded-index Si1-xGex waveguides with broadband tight mode confinement and flat anomalous dispersion for nonlinear mid-infrared photonicsJ M Ramirez, V Vakarin, J Frigerio, et al.
Human Genetics|December 1, 1991
Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WASL D Notarangelo, O Parolini, F Porta, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female caseJ M Shipley, S Birdsall, J Clark, et al.
Journal of Molecular Biology|April 20, 1985
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosomeJ Wolfe, S M Darling, R P Erickson, et al.
Genomics|May 1, 1991
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3S P Kwan, T Lehner, T Hagemann, et al.
Human Genetics|May 1, 1992
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 betaG de Saint Basile, L D Notarangelo, C Bonaiti-Pellié, et al.
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