✦ LIBER ✦

Adult with an interstitial deletion of chromosome 10 [del(10)(q25.1q25.3)]: Overlap with Coffin-Lowry Syndrome

✍ Scribed by McCandless, Shawn E. ;Schwartz, Stuart ;Morrison, Stuart ;Garlapati, Krishnaiah ;Robin, Nathaniel H.

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 280 KB
Volume: 95
Category: Article
ISSN: 0148-7299
DOI: 10.1002/1096-8628(20001113)95:2<93::aid-ajmg1>3.0.co;2-b

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Multiple craniofacial anomalies associat

Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)

✍ Leichtman, Lawrence G. ;Strum, Daniel ;Brothman, Arthur R. 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 368 KB 👁 1 views

Molecular characterization of a patient

Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities

✍ Maria Descartes; Julie Zenger Hain; Michael Conklin; Judy Franklin; Fady M. Mikh 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 198 KB 👁 2 views

Complex MCA/MR syndrome associated with

Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1?q27)

✍ Vermeesch, Joris R. ;Fryns, Jean-Pierre 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 89 KB 👁 1 views

Terminal deletion of the long arm of chr

Terminal deletion of the long arm of chromosome 10: A new case with breakpoint in q25.3

✍ Petersen, Birgit; Strassburg, Hans-Michael; Feichtinger, Wolfgang; Kress, Wolfra 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 8 KB 👁 2 views

Since the first patient with partial deletion of the long arm of chromosome 10 was described in 1978, another 23 cases have been reported, with the breakpoint ranging from 10q23.3-26.2. To contribute further to the delineation of the monosomy 10qter syndrome, we describe a female child who, at age 3

Interstitial deletion of chromosome 10,

Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies

✍ Zenger-Hain, Julie L. ;Roberson, Jacquelyn ;Van Dyke, Daniel L. ;Weiss, Lester 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 246 KB

Two concurrent chromosomal aberrations i

Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale

✍ Tetsuya Kibe; Yuka Mori; Tohru Okanishi; Keiko Shimojima; Kenji Yokochi; Toshiyu 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 256 KB