14q32 deletion syndrome: a clinical report.

التفاصيل البيبلوغرافية
العنوان: 14q32 deletion syndrome: a clinical report.
المؤلفون: Youngs EL; Department of Psychiatry and Behavioral Sciences Department of Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, USA., Dasouki M, Butler MG
المصدر: Clinical dysmorphology [Clin Dysmorphol] 2012 Jan; Vol. 21 (1), pp. 42-44.
نوع المنشور: Case Reports; Letter
اللغة: English
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE
أسماء مطبوعة: Publication: London : Lippincott Williams & Wilkins
Original Publication: London, UK : Chapman & Hall, c1992-
مواضيع طبية MeSH: Chromosome Aberrations ; Chromosome Deletion ; Chromosomes, Human, Pair 14/genetics ; Facies ; Female ; Humans ; Infant ; Voice Disorders/genetics
مستخلص: Competing Interests: There are no conflict of interest.
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معلومات مُعتمدة: P30 HD002528 United States HD NICHD NIH HHS
SCR Disease Name: Chromosome 14q, partial deletions
تواريخ الأحداث: Date Created: 20111207 Date Completed: 20120601 Latest Revision: 20211021
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC5176015
DOI: 10.1097/MCD.0b013e328348d8d0
PMID: 22143351
قاعدة البيانات: MEDLINE
الوصف
تدمد:1473-5717
DOI:10.1097/MCD.0b013e328348d8d0