Exclusion of the chromosomal 1p21 region in a large pedigree with a phenotypic variant of type II autosomal dominant osteopetrosis
暂无分享,去创建一个
[1] J. Bollerslev,et al. Osteopetrosis. A genetic and epidemiological study. , 2008, Clinical genetics.
[2] A. Schulz,et al. Loss of the ClC-7 Chloride Channel Leads to Osteopetrosis in Mice and Man , 2001, Cell.
[3] W. Hul,et al. Further Evidence for Genetic Heterogeneity Within Type II Autosomal Dominant Osteopetrosis , 2000, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[4] L. Notarangelo,et al. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis , 2000, Nature Genetics.
[5] T. Foroud,et al. Locus heterogeneity of autosomal dominant osteopetrosis (ADO). , 1999, The Journal of clinical endocrinology and metabolism.
[6] W. Hul,et al. Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21. , 1997, American journal of human genetics.
[7] B. Mevåg,et al. Identification by DNA analysis of the victims of the August 1996 Spitsbergen civil aircraft disaster , 1997, Nature Genetics.
[8] J. Ladenson,et al. Creatine kinase brain isoenzyme (BB‐CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders , 1996, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[9] Cécile Fizames,et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites , 1996, Nature.
[10] M. Cecchini,et al. Recent developments in the understanding of the pathophysiology of osteopetrosis. , 1996, European journal of endocrinology.
[11] J. O’Connell,et al. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritance , 1995, Nature Genetics.
[12] A. Jeffreys,et al. A somatic BRCA1 mutation in an ovarian tumour , 1995, Nature Genetics.
[13] D. Stoker,et al. Benign osteopetrosis: a review of 42 cases showing two different platterns , 1993, Skeletal radiology.
[14] F. Shapiro. Osteopetrosis. Current clinical considerations. , 1993 .
[15] J. W. Pendleton,et al. Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis Type II — a family study , 1992, Clinical genetics.
[16] J. Bollerslev. Autosomal dominant osteopetrosis: bone metabolism and epidemiological, clinical, and hormonal aspects. , 1989, Endocrine reviews.
[17] G. Lathrop,et al. Easy calculations of lod scores and genetic risks on small computers. , 1984, American journal of human genetics.
[18] D. Hewett‐Emmett,et al. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[19] R. Berger,et al. Partial 7q trisomy , 1977, Clinical genetics.
[20] F. Vellios,et al. OSTEOPETROSIS: A Clinical, Genetic, Metabolic, and Morphologic Study of the Dominantly Inherited, Benign Form , 1968 .
[21] F. Salzano. Osteopetrosis: review of dominant cases and frequency in a Brazilian state. , 1961, Acta geneticae medicae et gemellologiae.
[22] R. Abbay. The Shadow of Adam's Peak , 1887, Nature.
[23] J. Laredo,et al. Type II autosomal dominant osteopetrosis (Albers-Schönberg disease): clinical and radiological manifestations in 42 patients. , 2000, Bone.
[24] A. Massengill,et al. C2–3 facet joint ”pseudo-fusion”: anatomic basis of a normal variant , 1997, Skeletal Radiology.
[25] C. Kovacs,et al. Centrifugal osteopetrosis: appendicular sclerosis with relative sparing of the vertebrae , 1995, Skeletal radiology.
[26] A. Parfitt,et al. Plasma calcium control at quiescent bone surfaces: a new approach to the homeostatic function of bone lining cells. , 1989, Bone.