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Human Genetics|January 1, 1991
Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markersA Sefiani, R M'rad, L Simard, et al.Human Genetics|April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesLane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.Human Genetics|August 31, 1978
GM1-gangliosidosis: accumulation of ganglioside GM1 in cultured skin fibroblasts and correlation with clinical typesY Suzuki, N Nakamura, K FukuokaHuman Genetics|August 30, 1976
Familial occurrence of gonadal tumors in XY females with breast developmentK BoczkowskiHuman Genetics|December 18, 1998
A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous diseaseM Tsuda, M Kaneda, T Sakiyama, et al.Human Genetics|December 18, 1998
Alternative splicing of exons 29 and 30 in the neurofibromatosis type 1 geneV M Park, K A Kenwright, D B Sturtevant, et al.Human Genetics|December 18, 1998
In vivo somatic mutations in Werner's syndromeS Kyoizumi, Y Kusunoki, T Seyama, et al.Human Genetics|December 18, 1998
Selective complement C1s deficiency caused by homozygous four-base deletion in the C1s geneN Inoue, T Saito, R Masuda, et al.Human Genetics|December 18, 1998
The polymorphic 43Thr bcl-2 protein confers relative resistance to autoimmunity: an analytical evaluationS Komaki, M Kohno, N Matsuura, et al.Human Genetics|December 18, 1998
Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of XpB Fritz, W Küster, K H Orstavik, et al.Pageof 957