✦ LIBER ✦

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia

✍ Scribed by Jason Neal; Kira Apse; Mustafa Sahin; Christopher A. Walsh; Volney L. Sheen

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 120 KB
Volume: 140A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31334

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Bilateral perisylvian polymicrogyria, pe

Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5–11.1 Mb terminal deletion of 1p36

✍ Shoji Saito; Rie Kawamura; Tomoki Kosho; Takashi Shimizu; Koki Aoyama; Kenichi K 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 206 KB 👁 2 views

OEIS complex associated with chromosome

OEIS complex associated with chromosome 1p36 deletion: A case report and review

✍ Ayman W. El-Hattab; Josh C. Skorupski; Michael H. Hsieh; Amy M Breman; Ankita Pa 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 174 KB 👁 2 views

Partial deletion of chromosome 12q is no

Partial deletion of chromosome 12q is not usually associated with CFC syndrome

✍ Zollino, Marcella ;Neri, Giovanni 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 42 KB 👁 1 views

Refined FISH characterization of a de no

Refined FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome

✍ Finelli, Palma ;Giardino, Daniela ;Russo, Silvia ;Gottardi, Giulietta ;Cogliati, 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB 👁 3 views

Allelic loss on chromosome 1p is Associa

Allelic loss on chromosome 1p is Associated with progression and lymph node metastasis of primary breast carcinoma

✍ Kazuhiro Tsukamoto; Noriko Ito; Masataka Yoshimoto; Fujio Kasumi; Futoshi Akiyam 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 2 views

observed in a wide variety of human tumors. Cytogenetic and molecular genetic studies in breast carcinomas

?Tandem? duplication of 4p16.1p16.3 chro

?Tandem? duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype

✍ Zollino, M.; Wright, T.J.; Di Stefano, C.; Tosolini, A.; Battaglia, A.; Altherr, 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 29 KB 👁 1 views

Chromosome imbalance affecting the short arm of chromosome 4 results in a variety of distinct clinical conditions. Most of them share a number of manifestations, such as mental retardation, microcephaly, pre-and post-natal growth retardation, anteverted and low-set ears, that can be considered as no