𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Non-specific X-linked mental retardation: Linkage analysis in MRX2 and MRX4 families revisited

✍ Scribed by Hu, Ling-Jia ;Blumenfeld-Heyberger, Sandra ;Hanauer, André ;Weissenbach, Jean ;Mandel, Jean-Louis

Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
577 KB
Volume
51
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Four families (MRX43, MRX44, MRX45, MRX5
Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: Clinical and psychometric data and results of linkage analysis
✍ Hamel, Ben C.J.; Smits, Arie P.T.; van den Helm, Bellinda; Smeets, Dominique F.C 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 185 KB 👁 1 views

Four families are described in which mental retardation segregates in an X-linked fashion. Mental retardation was the only consistent clinical finding in all affected males. The degree of retardation varied from mild to profound both between and within families. Linkage analysis localized the geneti

X-linked nonspecific mental retardation
X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: The European XLMR consortium
✍ des Portes, Vincent; Beldjord, Ch�rif; Chelly, Jamel; Hamel, Ben; Kremer, Hannie 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 33 KB 👁 2 views

The identification of X-linked mental retardation genes (XLMR) represents a challenge of considerable medical importance, given the reported high cumulative frequency of this heterogenous disorder, estimated at approximately 1/600 male births. Whereas pooling families is useful to fine-map genetic l

Linkage analysis in three families with
Linkage analysis in three families with nonspecific X-linked mental retardation
✍ Claes, S.; Gu, X. X.; Legius, E.; Lorenzetti, E.; Marynen, P.; Fryns, J. P.; Cas 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 155 KB

Nonspecific X-linked mental retardation (XLMR) is a common disorder. The number of genes involved in this condition is not known, but it is estimated to be more than 10. We present a clinical and linkage study on 3 families with XLMR. All families were analyzed using highly polymorphic markers cover