A ring chromosome No. 16 in primary hypoparathyroidism
暂无分享,去创建一个
[1] S. Waxman,et al. Trisomy-16 in a mosaic carrier father and his aborted foetus. , 1969, Journal of medical genetics.
[2] V. McKusick,et al. Probable assignment of the Duffy blood group locus to chromosome 1 in man. , 1968, Proceedings of the National Academy of Sciences of the United States of America.
[3] M. N. Crawford,et al. Deletion of the Long Arm of Chromosome 16 and an Unexpected Duffy Blood Group Phenotype reveal a Possible Autosomal Linkage , 1967, Nature.
[4] L. Taitz,et al. Congenital absence of the parathyroid and thymus glands in an infant. (3 and 4 pharyngeal pouch syndrome). , 1966, Pediatrics.
[5] R. Blizzard,et al. The incidence of parathyroid and other antibodies in the sera of patients with idiopathic hypoparathyroidism. , 1966, Clinical and experimental immunology.
[6] D. Carr. Chromosome Studies in Spontaneous Abortions , 1965, Obstetrics and gynecology.
[7] R. Poulding,et al. Trisomy of Autosome 16 , 1963, Nature.
[8] I. Uchida,et al. Ring Chromosomes in Human Beings , 1962, Nature.
[9] I. Kopin,et al. Idiopathic hypoparathyroidism: report of a case with autopsy findings. , 1960, Annals of internal medicine.
[10] V. Peden. True idiopathic hypoparathyroidism as a sexlinked recessive trait. , 1960, American journal of human genetics.
[11] S. Farber,et al. CLINICAL pathological conference. , 1959, Clinical proceedings - Children's Hospital of the District of Columbia.