A ring chromosome No. 16 in an infant with primary hypoparathyroidism
J Pediatr
.
1970 May;76(5):745-51.
doi: 10.1016/s0022-3476(70)80295-5.
Authors
E Pergament
,
G C Pietra
,
T Kadotani
,
H Sato
,
S Berlow
PMID:
5440360
DOI:
10.1016/s0022-3476(70)80295-5
No abstract available
Publication types
Case Reports
MeSH terms
Abnormalities, Multiple
Chromosome Aberrations*
Chromosome Disorders*
Chromosomes, Human, 16-18*
Humans
Hypoparathyroidism / genetics*
Infant
Infant, Newborn
Karyotyping
Male
Pedigree