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Letter to the editor: Refined localization of the Prieto‐Syndrome locus

Letter to the editor: Refined localization of the Prieto‐Syndrome locus References Fain PR , Kort EN , Chance PF , Nguyen K , Reed DF , Econs MJ , Barker DF ( 1995 ): A 2D crossover‐based map of the human X chromosome as a model for map integration . Nature Genet 9 : 261 – 266 . Gyapay G , Morissette J , Vignal A , Dib C , Fizames C , Millaseau P , Marc S , Bernardi G , Lathrop M , Weissenbach J ( 1994 ): The 1993–1994 Généthon human genetic linkage map . Nature Genet 7 : 246 – 339 . Hendriks RW , Chen Z‐Y , Hinds H , Schuurman RKB , Craig IW , ( 1992 ): An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene . Hum Molec Genet 1 ( 3 ): 187 – 194 . Kirchgessner CU , Trofatter JA , Mahtani MM , Willard HF , De Gennaro LJ ( 1991 ): A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the Synapsin I/A‐raf‐I genes . Am J Hum Genet 49 : 184 – 191 . Moore B , Kwan S‐P , Bech‐Hansen NT ( 1992 ): A polymorphic dinucleotide repeat at the DXS7 locus . Nucleic Acid Res 20 : 929 . Prieto F , Badía L , Mulas F , Monford A , Mora F , ( 1987 ): X‐linked dysmorphic syndrome with mental retardation . Clin Genet 32 : 326 – 334 . Watty A , Prieto F , Beneyto M , Neugebauer M , Gal A ( 1991 ): Gene localization in a family with X‐linked syndromal mental retardation (Prieto syndrome) . Am J Med Genet 38 : 234 – 239 . http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png American Journal of Medical Genetics Part A Wiley

Letter to the editor: Refined localization of the Prieto‐Syndrome locus

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References (8)

Publisher
Wiley
Copyright
Copyright © 1996 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1552-4825
eISSN
1552-4833
DOI
10.1002/(SICI)1096-8628(19960712)64:1<82::AID-AJMG14>3.0.CO;2-O
pmid
8826455
Publisher site
See Article on Publisher Site

Abstract

References Fain PR , Kort EN , Chance PF , Nguyen K , Reed DF , Econs MJ , Barker DF ( 1995 ): A 2D crossover‐based map of the human X chromosome as a model for map integration . Nature Genet 9 : 261 – 266 . Gyapay G , Morissette J , Vignal A , Dib C , Fizames C , Millaseau P , Marc S , Bernardi G , Lathrop M , Weissenbach J ( 1994 ): The 1993–1994 Généthon human genetic linkage map . Nature Genet 7 : 246 – 339 . Hendriks RW , Chen Z‐Y , Hinds H , Schuurman RKB , Craig IW , ( 1992 ): An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene . Hum Molec Genet 1 ( 3 ): 187 – 194 . Kirchgessner CU , Trofatter JA , Mahtani MM , Willard HF , De Gennaro LJ ( 1991 ): A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the Synapsin I/A‐raf‐I genes . Am J Hum Genet 49 : 184 – 191 . Moore B , Kwan S‐P , Bech‐Hansen NT ( 1992 ): A polymorphic dinucleotide repeat at the DXS7 locus . Nucleic Acid Res 20 : 929 . Prieto F , Badía L , Mulas F , Monford A , Mora F , ( 1987 ): X‐linked dysmorphic syndrome with mental retardation . Clin Genet 32 : 326 – 334 . Watty A , Prieto F , Beneyto M , Neugebauer M , Gal A ( 1991 ): Gene localization in a family with X‐linked syndromal mental retardation (Prieto syndrome) . Am J Med Genet 38 : 234 – 239 .

Journal

American Journal of Medical Genetics Part AWiley

Published: Dec 12, 1996

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