✦ LIBER ✦

Down syndrome (trisomy 21) with premaxillary agenesis and semilobar holoprosencephaly

✍ Scribed by Sriparna Basu; Ashok Kumar; B.K. Das

Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 133 KB
Volume: 149A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.33072

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Hematologic disorders in 13 patients wit

Hematologic disorders in 13 patients with acquired trisomy 21 and 13 individuals with Down syndrome

✍ Dewald, Gordon W. ;Diez-Martin, Jose L. ;Steffen, Sara L. ;Jenkins, Robert B. ;S 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 339 KB 👁 2 views

A girl with Down syndrome and partial tr

A girl with Down syndrome and partial trisomy for 21pter-q22.13: A clue to narrow the Down syndrome critical region

✍ Daisuke Sato; Hiroki Kawara; Osamu Shimokawa; Naoki Harada; Hidefumi Tonoki; Nob 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 201 KB 👁 2 views

Risk of Down's syndrome among second- an

Risk of Down's syndrome among second- and third-degree relatives of a proband with trisomy 21

✍ ten Kate, Leo P. ;te Meerman, Gerard J. ;Anders, G. J. P. A. 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 94 KB 👁 2 views

Clinical, cytogenetic, and molecular eva

Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype

✍ Williams, Charles A. ;Frias, Jaime L. ;McCormick, Mary Kay ;Antonarakis, Stylian 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 491 KB 👁 2 views

Down syndrome with biparental inheritanc

Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: Confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysis

✍ Rajangam, Sayee; Michaelis, Ron C.; Velagaleti, GopalRao V. N.; Lincoln, Shavant 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 306 KB 👁 2 views

## Individuals with translocation Down syndrome (DS) often inherit the rearranged chromosome from a carrier parent. DS due to inheritance of one Robertsonian or derivative (14q21q) from one parent and a second der(14q21q) in addition to a free chromosome 21 from the other parent are rarely documen