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congenital absence of vermilion 相关文献:
Coffin-Siris Syndrome.
Schrier Vergano S, Santen G, Wieczorek D, Matsumoto N.
2013 Apr 4 [updated 2025 May 15]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:23556151
Single Surgeon's Experience in Repair of Median Cleft Lip: A Case Series of 5 Median Craniofacial Dysplasia Patients.
Yoo H, Ha JH, Chung JH, Kim S.
J Craniofac Surg. 2023 Jan-Feb 01;34(1):318-321. doi: 10.1097/SCS.0000000000008929. Epub 2022 Aug 17.
PMID:36608084
Exome sequencing identifies de novo pathogenic variants in FBN1TRPS1 in a patient with a complex connective tissue phenotype.
Zastrow DB, Zornio PA, Dries A, Kohler J, Fernandez L, Waggott D, Walkiewicz M, Eng CM, Manning MA, Farrelly E; Undiagnosed Diseases Network; Fisher PG, Ashley EA, Bernstein JA, Wheeler MT.
Cold Spring Harb Mol Case Stud. 2017 Jan;3(1):a001388. doi: 10.1101/mcs.a001388.
PMID:28050602
Pulmonary venous blood flow pattern in patients with univentricular hearts following total cavo-pulmonary connection.
Rydberg A, Teien DE, Karp K, Vermilion RP, Ludomirsky A.
Clin Physiol. 1998 Mar;18(2):131-8. doi: 10.1046/j.1365-2281.1998.00086.x.
PMID:9568352
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