推官网,引流量

直推官网引流,大量子站导流 效果持久显著

批量建站,提收录

形成站群推广模式 让搜索引擎大量收录!

提权重,树权威

实现权重提升 树立行业权威

部署快,自主可控

免费下载

省成本,提效率

多分站齐推广,性价比高 批量数据分析,帮助及时调整优化

关于OD
关于OD
5月16日晚,昆山奥体中心,江苏足球超等联赛迎来精彩对决,苏州队镇守主场迎战连云
关于OD
188金宝博官网app下载 5月16日晚,苏超苏州主场迎战连云港,上海戏校校长、
关于OD
北京时刻5月20日凌晨1点,2026年谷歌I/O大会矜重演出,AI依旧是弥散的主
【【【序论:iQOO的数字系列旗舰,迎来了新成员】】】 无人不晓,在iQOO的旗
本翰墨数:1294,阅读时长简短2分钟 作家|第一财经何涛 封图|“耿同学讲故事
5月15日,英伟达CEO黄仁勋现身北京南锣饱读巷吃炸酱面,高清镜头捕捉到其指甲灰

OD资讯

ODZIXUN

OD资讯

查看更多
  • OD体育

    OD体育

  • 关于OD

    关于OD

  • OD资讯

    OD资讯

  • OD盘口

    OD盘口

OD盘口

  • OD盘口

OD体育(ODSports)官网入口

临床医学名词词典
首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
neonatal wide cranial sutures相关文献:
Wide sutures and large fontanels in the newborn.
Tan KL.
Am J Dis Child. 1976 Apr;130(4):386-90. doi: 10.1001/archpedi.1976.02120050044007.
PMID:1266823
Yunis Varon syndrome.
Kulkarni ML, Vani HN, Nagendra K, Mahesh TK, Kumar A, Haneef S, Mohammed Z, Kulkarni PM.
Indian J Pediatr. 2006 Apr;73(4):353-5. doi: 10.1007/BF02825832.
PMID:16816498
Hypophosphatasia in a newborn infant.
Tekinalp G, Yükselen A, Balkanci F, Coşkun T, Yurdakök M.
Turk J Pediatr. 1995 Jan-Mar;37(1):61-5.
PMID:7732610
3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome).
Verloes A, Dresse MF, Jovanovic M, Dodinval P, Geubelle F.
Clin Genet. 1989 Mar;35(3):205-8. doi: 10.1111/j.1399-0004.1989.tb02929.x.
PMID:2650935
A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasia.
Cisarova K, Garavelli L, Caraffi SG, Peluso F, Valeri L, Gargano G, Gavioli S, Trimarchi G, Neri A, Campos-Xavier B, Superti-Furga A.
Am J Med Genet A. 2022 Jan;188(1):319-325. doi: 10.1002/ajmg.a.62506. Epub 2021 Sep 28.
PMID:34580982
A review of hedgehog signaling in cranial bone development.
Pan A, Chang L, Nguyen A, James AW.
Front Physiol. 2013 Apr 2;4:61. doi: 10.3389/fphys.2013.00061. eCollection 2013.
PMID:23565096
Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature.
Tonni G, Panteghini M, Rossi A, Baldi M, Magnani C, Ferrari B, Lituania M.
Arch Gynecol Obstet. 2011 Apr;283(4):909-16. doi: 10.1007/s00404-010-1643-6. Epub 2010 Sep 2.
PMID:20811900
Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?
Faria ÁC, Rabbi-Bortolini E, Rebouças MRGO, de S Thiago Pereira ALA, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV.
Am J Med Genet A. 2016 Feb;170A(2):403-409. doi: 10.1002/ajmg.a.37448. Epub 2015 Nov 14.
PMID:26566760
Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB.
Goto T, Aramaki M, Yoshihashi H, Nishimura G, Hasegawa Y, Takahashi T, Ishii T, Fukushima Y, Kosaki K.
Congenit Anom (Kyoto). 2004 Dec;44(4):225-9. doi: 10.1111/j.1741-4520.2004.00043.x.
PMID:15566413
An unusually-wide human bregmatic Wormian bone: anatomy, tomographic description, and possible significance.
Barberini F, Bruner E, Cartolari R, Franchitto G, Heyn R, Ricci F, Manzi G.
Surg Radiol Anat. 2008 Nov;30(8):683-7. doi: 10.1007/s00276-008-0371-0. Epub 2008 Jun 4.
PMID:18523715
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3