Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Works matching IS 09185739 AND DT 2015 AND VI 24 AND IP 1
Results: 5
1
2
Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 1, p. 27, doi. 10.1297/cpe.24.27
- By:
- Publication type:
- Article
3
Onset of puberty and near adult height in short children born small for gestational age and treated with GH: Interim analysis of up to 10 years of treatment in Japan.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 1, p. 15, doi. 10.1297/cpe.24.15
- By:
- Publication type:
- Article
4
A 45,X/46,XY DSD (Disorder of Sexual Development) case with an extremely uneven distribution of 46,XY cells between lymphocytes and gonads.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
5
Growth failure starts from early infancy in children with short stature at age 6.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 1, p. 1, doi. 10.1297/cpe.24.1
- By:
- Publication type:
- Article