التفاصيل البيبلوغرافية
| العنوان: |
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort. |
| المؤلفون: |
van der Sluijs PJ, Joosten M, Alby C, Attié-Bitach T, Gilmore K, Dubourg C, Fradin M, Wang T, Kurtz-Nelson EC, Ahlers KP, Arts P, Barnett CP, Ashfaq M, Baban A, van den Born M, Borrie S, Busa T, Byrne A, Carriero M, Cesario C, Chong K, Cueto-González AM, Dempsey JC, Diderich KEM, Doherty D, Farholt S, Gerkes EH, Gorokhova S, Govaerts LCP, Gregersen PA, Hickey SE, Lefebvre M, Mari F, Martinovic J, Northrup H, O'Leary M, Parbhoo K, Patrier S, Popp B, Santos-Simarro F, Stoltenburg C, Thauvin-Robinet C, Thompson E, Vulto-van Silfhout AT, Zahir FR, Scott HS, Earl RK, Eichler EE, Vora NL, Wilnai Y, Giordano JL, Wapner RJ, Rosenfeld JA, Haak MC, Santen GWE |
| المصدر: |
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Feb; Vol. 25 (2), pp. 100004. |
| نوع المنشور: |
Published Erratum |
| اللغة: |
English |
| بيانات الدورية: |
Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: PubMed not MEDLINE; MEDLINE |
| أسماء مطبوعة: |
Publication: 2022- : [New York] : Elsevier
Original Publication: Baltimore, MD : Lippincott, Williams & Wilkins, c1998- |
| التعليقات: |
Erratum for: Genet Med. 2022 Aug;24(8):1753-1760. (PMID: 35579625) |
| معلومات مُعتمدة: |
P50 HD103524 United States HD NICHD NIH HHS; R01 MH101221 United States MH NIMH NIH HHS |
| تواريخ الأحداث: |
Date Created: 20230206 Latest Revision: 20240322 |
| رمز التحديث: |
20240322 |
| مُعرف محوري في PubMed: |
PMC9983121 |
| DOI: |
10.1016/j.gim.2022.100004 |
| PMID: |
36745127 |
| قاعدة البيانات: |
MEDLINE |
