A ring chromosome No. 16 in primary hypoparathyroidism

[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.