✦ LIBER ✦

Vasomotor instability in neonates with chromosome 22q11 deletion syndrome

✍ Scribed by Shashi, Vandana ;Berry, Margaret N. ;Hines, Michael H.

Publisher: John Wiley and Sons
Year: 2003
Tongue: English
Weight: 56 KB
Volume: 121A
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.a.20219

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Sclerocornea associated with the chromos

Sclerocornea associated with the chromosome 22q11.2 deletion syndrome

✍ Gil Binenbaum; Donna M. McDonald-McGinn; Elaine H. Zackai; B. Michael Walker; Ka 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 76 KB 👁 2 views

Malignancy in chromosome 22q11.2 deletio

Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

✍ Donna M. McDonald-McGinn; Anne Reilly; Carina Wallgren-Pettersson; H. Eugene Hoy 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 77 KB 👁 3 views

22q11 deletion syndrome in adults with s

22q11 deletion syndrome in adults with schizophrenia

✍ Bassett, Anne S.; Hodgkinson, Kathy; Chow, Eva W.C.; Correia, Susana; Scutt, Lau 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 48 KB 👁 3 views

Genetic syndromes associated with deletions at chromosome 22q11 generally have been diagnosed during childhood based on a constellation of physical features. To investigate a reported association of velocardiofacial syndrome with psychotic disorders in adults, we assessed subjects with DSM-IV schizo

Chromosome 22q11.2 deletion in a boy wit

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome

✍ Fryburg, Julie S.; Lin, Kant Y.; Golden, Wendy L. 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 7 KB 👁 2 views

This report is on a 14-month-old boy with manifestations of Opitz (G/BBB) syndrome in whom a 22q11.2 deletion was found. Deletion analysis was requested because of some findings in this patient reminiscent of velocardiofacial (VCF) syndrome. The extent of aspiration and of respiratory symptoms in th

Kousseff syndrome caused by deletion of

Kousseff syndrome caused by deletion of chromosome 22q11-13

✍ Forrester, Shawnia ;Kovach, Margaret J. ;Smith, Randell E. ;Rimer, Lisa ;Wesson, 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 117 KB 👁 1 views

Type I diabetes mellitus in a patient wi

Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome

✍ Elder, Deborah A. ;Kaiser-Rogers, Kathleen ;Aylsworth, Arthur S. ;Calikoglu, Ali 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 76 KB 👁 1 views

We describe a patient with type I diabetes, clinical ®ndings consistent with velocardiofacial syndrome, and a chromosome 22q11.2 deletion. A nine-year-old boy presented with a history of polyuria, polydipsia, weight loss, hyperglycemia, ketosis, serum insulin antibodies, and a low C-peptide level. H