지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2015.1
- 수록면
- 275 - 278 (4page)
이용수
초록· 키워드
오류제보하기
등록된 정보가 없습니다.
목차
등록된 정보가 없습니다.
참고문헌 (10)
참고문헌 신청
Balasubramanian M / 2011 / Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype / J Med Genet 48 : 290 ~ 298
Docker D / 2014 / Further delineation of the SATB2 phenotype / Eur J Hum Genet 22 : 1034 ~ 1039
FitzPatrick DR / 2003 / Identification of SATB2 as the cleft palate gene on 2q32-q33 / Hum Mol Genet 12 : 2491 ~ 2501
Miller DT / 2010 / Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalie
Nicholl J / 2014 / Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH / Pathology 46 : 41 ~ 45
Docker D / 2014 / Further delineation of the SATB2 phenotype / Eur J Hum Genet 22 : 1034 ~ 1039
FitzPatrick DR / 2003 / Identification of SATB2 as the cleft palate gene on 2q32-q33 / Hum Mol Genet 12 : 2491 ~ 2501
Miller DT / 2010 / Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalie
Nicholl J / 2014 / Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH / Pathology 46 : 41 ~ 45
함께 읽어보면 좋을 논문
논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
-
Special AT-rich sequence-binding protein 2 (SATB2) in the differential diagnosis of osteogenic and non-osteogenic bone and soft tissue tumors
Journal of Pathology and Translational Medicine
2022 .09
-
MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report
Annals of Rehabilitation Medicine
2015 .01
-
1q21.1 microdeletion identified by chromosomal microarray in a newborn with upper airway obstruction
Journal of genetic medicine
2018 .01
-
The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome
Annals of Pediatirc Endocrinology & Metabolism
2024 .02
-
Genetic Screening for Chromosomal Abnormalities and Y Chromosome Microdeletions in 846 Infertile Korean Men
Laboratory Medicine Online
2018 .01
-
An analysis of Y-chromosome microdeletion in infertile Korean men with severe oligozoospermia or azoospermia
Investigative and Clinical Urology
2024 .01
-
Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion
Annals of Pediatirc Endocrinology & Metabolism
2015 .01
-
A case of CHARGE syndrome featuring immunodeficiency and hypocalcemia
Journal of genetic medicine
2015 .01
-
Vascular compression syndromes: a pictorial review
ULTRASONOGRAPHY
2022 .07
-
14q12q13.3 Deletion Diagnosed Using Chromosomal Microarray Analysis in an Infant Showing Seizures, Hypoplasia of the Corpus Callosum, and Developmental Delay
Neonatal medicine
2020 .01
-
Genetic overgrowth syndrome: A single center's experience
Journal of genetic medicine
2018 .01
-
尹吉榮의 病證 대분류에 대한 고찰
대한한의진단학회지
2015 .01
-
Does wastewater discharge have relations with increase of Turner syndrome and Down syndrome?
Environmental Analysis Health and Toxicology
2017 .12
-
한열변증 점수를 이용한 한증과 열증의 건강 상태와 미병 특징 비교
대한한의학회지
2018 .03
-
Chromosome 11q13 deletion syndrome
Clinical and Experimental Pediatrics
2016 .01
-
Concurrent SHORT syndrome and 3q duplication syndrome
Journal of genetic medicine
2019 .01
-
A boy with 46,X,+mar presenting gynecomastia and short stature
Annals of Pediatirc Endocrinology & Metabolism
2017 .01
-
1p36 Deletion syndrome Presenting with Various Epileptic Semiologies
대한소아신경학회지
2015 .12
-
한의학 학술지에 게재된 안구건조증에 대한 논문 고찰
동의생리병리학회지
2017 .01
-
한의학 학술지에 게재된 안구건조증에 대한 논문 고찰
동의생리병리학회지
2017 .04
이 논문의 저자 정보
최근 본 자료
댓글(0)
0