✦ LIBER ✦

Genetic Analysis in the Diagnosis of Familial Paragangliomas

✍ Scribed by Anna E. Petropoulos; Charles M. Luetje; Paul J. Camarata; C. Keith Whittaker; Graham Lee; Bora E. Baysal

Book ID: 110082371
Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 26 KB
Volume: 110
Category: Article
ISSN: 0023-852X
DOI: 10.1097/00005537-200007000-00030

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Molecular genetic diagnosis of familial

Molecular genetic diagnosis of familial tumors

✍ Naohiro Tomita; Michiei Oto 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 396 KB

Genetic analysis of familial erythrophag

Genetic analysis of familial erythrophagocytic lymphohistiocytosis

✍ A. Gencik; E. Signer; Hj. Müller 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 399 KB

Cytogenetic analysis of tissues from pat

Cytogenetic analysis of tissues from patients with familial paragangliomas of the head and neck

✍ Dr. Ann-Leslie Zaslav; Dr. David Myssiorek; Dr. Christina Mucia; Dr. Joyce E. Fo 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 547 KB

Background. Paragangliomas of the head and neck are slow-growing tumors that originate from neural crest cells. Between 7% and 9% of these tumors have a familial occurrence. The suspected gene for familial paragangliomas (FP) is transmitted with an autosomal dominant mode of inheritance with incompl

The genetics of paragangliomas: a review

✍ Martin T.P.C.; Irving R.M.; Maher E.R. 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 546 KB

Molecular genetic diagnosis of the famil

Molecular genetic diagnosis of the familial myxoma syndrome (Carney complex)

✍ Goldstein, Marsha M.; Casey, Mairead; Carney, J. Aidan; Basson, Craig T. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 18 KB 👁 2 views

We describe an individual in whom molecular genetic testing provided a diagnosis of the Carney complex, an autosomal dominant syndrome comprising cutaneous and cardiac myxomas, spotty pigmentation of the skin, and endocrinopathy. Recently, we localized the Carney complex disease gene to chromosome r

A novel mutation in the SDHD gene in a f

A novel mutation in the SDHD gene in a family with inherited paragangliomas—implications of genetic diagnosis for follow up and treatment

✍ Laurette Renard; Catherine Godfraind; Laurence M. Boon; Miikka Vikkula 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 188 KB

## Abstract ## Background. Early detection of paragangliomas (PGs) has been linked to low morbidity after surgical resection. Recent identification of causative genes (__SDHB, SDHC,__ and __SDHD__) has made it possible to detect individuals at high risk for tumors. ## Methods. We identified a th