✦ LIBER ✦

Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome

✍ Scribed by Gisele da Silva Dalben; Antonio Richieri-Costa; Luís Antônio de Assis Taveira

Book ID: 116942282
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 357 KB
Volume: 106
Category: Article
ISSN: 1528-395X
DOI: 10.1016/j.tripleo.2008.04.019

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Tooth abnormalities and soft tissue alte

Tooth abnormalities and soft tissue alterations in patients with G/BBB syndrome

✍ G Da Silva Dalben; A Richieri-Costa; LA De Assis Taveira 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 359 KB

Dental development and tooth agenesis in

Dental development and tooth agenesis in children with velocardiofacial syndrome

✍ ARJA HELIÖVAARA; IRMA RANTANEN; SIRPA ARTE 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 67 KB

Bone and soft tissue changes in parapleg

Bone and soft tissue changes in paraplegic patients

✍ Hancock, D A ;Reed, G W ;Atkinson, P J ;Cook, J B ;Smith, P H 📂 Article 📅 1979 🏛 Nature Publishing Group 🌐 English ⚖ 186 KB

Obsessive-compulsive disorder in patient

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

✍ Gothelf, Doron ;Presburger, Gadi ;Zohar, Ada H. ;Burg, Merav ;Nahmani, Ariela ;F 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 81 KB 👁 3 views

Allergies in patients with chromosome 22

Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease

✍ Lauren Staple; Timothy Andrews; Donna McDonald-McGinn; Elaine Zackai; Kathleen E 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 90 KB

Chromosome 22q11.2 microdeletions in vel

Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations

✍ Ravnan, J. Britt; Chen, Emily; Golabi, Mahin; Lebo, Roger V. 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 677 KB

Vtalocardiofacial syndrome (VCFS) and the DiGeorge sequence (DGS) are caused by 22q11.2 deletions. Fluorescence in situ hybisidization (FISH) using the DiGeorge chromosome region (DGCR) probe (Oncor) was used to detect 31 deletions in 100 patients with possible VCFS. Retrospective FISH analysis of a