✦ LIBER ✦

del(15)(q22q24) Syndrome with Potter sequence

✍ Scribed by Clark, Robin Dawn

Publisher: John Wiley and Sons
Year: 1984
Tongue: English
Weight: 142 KB
Volume: 19
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320190409

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Del(10)(q22.3q24.1) associated with juve

Del(10)(q22.3q24.1) associated with juvenile polyposis

✍ Jacoby, Russell F.; Schlack, Steven; Sekhon, Gurbax; Laxova, Renata 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB

Juvenile polyps are the most frequent gastrointestinal polyps with a malignant potential for which the genetic basis is unknown. Juvenile polyps, with a normal epithelium but hypertrophic lamina propria, are histologically quite distinct from adenomatous polyps which have dysplastic changes in epith

Myelodysplastic syndrome in a child with

Myelodysplastic syndrome in a child with 15q24 deletion syndrome

✍ Yoko Narumi; Masaaki Shiohara; Keiko Wakui; Asahito Hama; Seiji Kojima; Kentaro 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 242 KB 👁 1 views

Craniosynostosis in an infant with an in

Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY,del(15)(q15q22.1)]

✍ Fukushima, Yoshimitsu ;Wakui, Keiko ;Nishida, Toshiro ;Nishimoto, Hiroshi 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 420 KB 👁 1 views

Mosaicism del(22)(q11.2q11.2)/dup(22)(q1

Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome

✍ Melissa A. Dempsey; Stuart Schwartz; Darrel J. Waggoner 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 172 KB 👁 1 views

Clinical and molecular characterization

Clinical and molecular characterization of a patient with Langer–Giedion syndrome and mosaic del(8)(q22.3q24.13)

✍ Alan L. Shanske; Ankita Patel; Sou Saukam; Brynn Levy; Hermann-Josef Lüdecke 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 254 KB 👁 2 views

The del(4) (q31) syndrome-A recognizable

The del(4) (q31) syndrome-A recognizable disorder with atypical Robin malformation Sequence

✍ Davis, Jeffrey M. ;Clarren, Sterling K. ;Salk, Darrell J. ;Opitz, John M. 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 287 KB

## Abstract Deletions of the terminal region of the long arm of chromosome 4 have been reported previously in 6 patients. With the addition of our patient with 46,XX,del(4) (pter→q31:), it becomes clearer that this is a recognizable syndrome. None of the 7 patients has had prenatal growth deficienc