X-linked Mental Retardation: in Pursuit of a Gene Map

Overview

Journal Am J Hum Genet

Publisher Cell Press

Specialty Genetics

Date 1993 Jun 1

PMID 8503437

Citations 6

Authors

C E Schwartz

Affiliations

Soon will be listed here.

Citing Articles

Tuber cinereum diverticula in a 28-month-old with xq21 deletion syndrome.

Whitehead M, Vezina G Case Rep Radiol. 2014; 2014:413574.

PMID: 25126438 PMC: 4122022. DOI: 10.1155/2014/413574.

X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.

Hahn K, Salomons G, Tackels-Horne D, Wood T, Taylor H, Schroer R Am J Hum Genet. 2002; 70(5):1349-56.

PMID: 11898126 PMC: 447610. DOI: 10.1086/340092.

Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.

Stevenson R, Hane B, Arena J, May M, Lawrence L, Lubs H J Med Genet. 1997; 34(6):465-9.

PMID: 9192265 PMC: 1050968. DOI: 10.1136/jmg.34.6.465.

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Gu X, Decorte R, Marynen P, Fryns J, Cassiman J, Raeymaekers P J Med Genet. 1996; 33(1):52-5.

PMID: 8825049 PMC: 1051812. DOI: 10.1136/jmg.33.1.52.

Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia.

Villard L, Toutain A, Lossi A, Gecz J, Houdayer C, Moraine C Am J Hum Genet. 1996; 58(3):499-505.

PMID: 8644709 PMC: 1914575.

References

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