서브메뉴
검색
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)
Detailed Information
- 자료유형
- 기사
- ISSN
- 87563282
- 저자명
- Bastepe, M.
- 서명/저자
- Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib) / Bastepe, M. , 공저 Altug-Teber, O. , Agarwal, C. , Oberfield, S. E. , Bonin, M. , Juppner, H.
- 발행사항
- Oxford : Elsevier Inc, 2011.
- 형태사항
- pp. 659-662
- 주기사항
- included reference
- 기타저자
- Altug-Teber, O.
- 기타저자
- Agarwal, C.
- 기타저자
- Oberfield, S. E.
- 기타저자
- Bonin, M.
- 기타저자
- Juppner, H.
- 원문정보
- url
- 모체레코드
- 모체정보확인
- Control Number
- kjul:60245291
MARC
008191120s2011 ai aa eng■022 ▼a87563282
■1001 ▼aBastepe, M.
■24510▼aPaternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)▼dBastepe, M.▼e공저 Altug-Teber, O.▼eAgarwal, C.▼eOberfield, S. E.▼eBonin, M.▼eJuppner, H.
■260 ▼aOxford▼bElsevier Inc▼c2011.
■300 ▼app. 659-662
■500 ▼aincluded reference
■7001 ▼aAltug-Teber, O.
■7001 ▼aAgarwal, C.
■7001 ▼aOberfield, S. E.
■7001 ▼aBonin, M.
■7001 ▼aJuppner, H.
■773 ▼tBone=International Bone and Mineral Society▼gVol. 48 No. 3 (2011. 3)▼d2011, 03
■856 ▼uhttp://www.elsevier.com/locate/bone
■SIS ▼aS057672▼b60077318▼h8▼s2▼fP
Preview
Export
ChatGPT Discussion
AI Recommended Related Books
detalle info
- Reserva
- No existe
- Mi carpeta
- Reference Materials for Thesis Writing
- Reference Materials for Research Ethics
- Job-Related Books
