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A. Watty, F. Prieto, M. Beneyto, M. Neugebauer, A. Gal (1991)
Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).American journal of medical genetics, 38 2-3
B. Moore, S. Kwan, N. Bech‐Hansen (1991)
A polymorphic dinucleotide repeat at the DXS7 locus.Nucleic acids research, 20 4
P. Fain, E. Kort, P. Chance, K. Nguyen, Douglas Redd, M. Econs, D. Barker (1995)
A 2D crossover–based map of the human X chromosome as a model for map integrationNature Genetics, 9
C. Kirchgessner, J. Trofatter, M. Mahtani, H. Willard, L. Degennaro (1991)
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes.American journal of human genetics, 49 1
R. Hendriks, Z. Chen, H. Hinds, R. Schuurman, I. Craig (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.Human molecular genetics, 1 8
D. Barker, J. Cleverly, P. Fain (1992)
Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22.Nucleic acids research, 20 4
G. Gyapay, J. Morissette, A. Vignal, C. Dib, C. Fizames, P. Millasseau, S. Marc, G. Bernardi, M. Lathrop, J. Weissenbach (1994)
The 1993–94 Généthon human genetic linkage mapNature Genetics, 7
F. Prieto, L. Badía, F. Mulas, A. Monfort, F. Mora (1987)
X‐linked dysmorphic syndrome with mental retardationClinical Genetics, 32
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 .
American Journal of Medical Genetics Part A – Wiley
Published: Dec 12, 1996
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