Osteopetrosis: a single centre experience of stem cell transplantation and prenatal diagnosis

Author:

Kapelushnik J,Shalev C,Yaniv I,Aker M,Carmi R,Cohen Z,Mozer A,Schulman C,Stein G,Or R

Publisher

Springer Science and Business Media LLC

Subject

Transplantation,Hematology

Reference18 articles.

1. Sly W . Carbonic Anhydrase deficiency syndrome: osteopetrosis with renal tubular acidosis and cerebral calcifications In: Scriver C, Beaudet A, Sly W, Valle D (eds) The Metabolic Basis of Inherited Disease McGraw-Hill: New York 1989 pp 2857–2866

2. Helfrich M, Aronson D, Everts V et al. Morphologic features of bone in human osteopetrosis Bone 1991 12: 411–419

3. van Hul W, Bollerslev J, Gram J et al. Localization of a gene for autosomal dominant osteopetrosis (Albers–Schonberg disease) to chromosome 1p2 Am J Hum Genet 1997 61: 363–369

4. Seiff CA, Chessels JM, Levinsky R . Allogenic bone-marrow transplantation in infantile malignant osteopetrosis Lancet 1983 1: 437–441

5. Gerritsen EJ, Vossen JM, Loo IHv et al. Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course Pediatrics 1994 93: 247–253

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