✦ LIBER ✦

Bilateral reactive lymphoid hyperplasia of the orbit in a child with Russell-Silver syndrome

✍ Scribed by Yen N.T. Dang; In C. Shin; Robert A. Gordon; Zeynel A. Karcioglu

Book ID: 116589348
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 257 KB
Volume: 8
Category: Article
ISSN: 1528-3933
DOI: 10.1016/j.jaapos.2004.09.005

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Rare case of exuberant benign lymphoid h

Rare case of exuberant benign lymphoid hyperplasia involving the conjunctiva, caruncle, and plica in a child with tonsilar enlargement

✍ Johnny Tang; I.Rand Rodgers; Kevin L Basham; Joan Goh 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 126 KB

Deletion of the paternal allele of the i

Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver–Russell syndrome features

✍ T Eggermann; S Spengler; M Begemann; G Binder; K Buiting; B Albrecht; S Spranger 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 484 KB

Deletions and rearrangements of the H19/

Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation

✍ Gronskov, K.; Poole, R. L.; Hahnemann, J. M. D.; Thomson, J.; Tumer, Z.; Brondum 📂 Article 📅 2011 🏛 BMJ Publishing Group 🌐 English ⚖ 546 KB

Epigenetic mutations of the imprinted IG

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

✍ Bartholdi, D. (author);Krajewska-Walasek, M. (author);Õunap, K. (author);Gaspar, 📂 Article 📅 2008 🏛 BMJ Publishing Group 🌐 English ⚖ 232 KB

Epigenetic mutations of the imprinted IG

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

✍ Bartholdi, D. (author);Krajewska-Walasek, M. (author);Õunap, K. (author);Gaspar, 📂 Article 📅 2008 🏛 BMJ Publishing Group 🌐 English ⚖ 232 KB

Co-occurrence of 4p16.3 deletions with b

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype

✍ Sarah T. South; Heidi Whitby; Teresa Maxwell; Emily Aston; Arthur R. Brothman; J 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 183 KB 👁 2 views