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114 related items for PubMed ID: 8826446

  • 1. Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings.
    Hamel BC, Smits AP, Otten BJ, van den Helm B, Ropers HH, Mariman EC.
    Am J Med Genet; 1996 Jul 12; 64(1):35-41. PubMed ID: 8826446
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  • 4. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
    Gedeon AK, Glass IA, Connor JM, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):121-4. PubMed ID: 8826461
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  • 5. X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11.
    Strømme P, Sundet K, Mørk C, Cassiman JJ, Fryns JP, Claes S.
    J Med Genet; 1999 May 12; 36(5):374-8. PubMed ID: 10353782
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  • 7. Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2.
    Bar-David S, Lerer I, Sarfaty CK, Kohan ZG, Meiner V, Zlotogora J, Abeliovich D.
    Am J Med Genet; 1996 Jul 12; 64(1):83-8. PubMed ID: 8826456
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  • 8. Linkage localization of Börjeson-Forssman-Lehmann syndrome.
    Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA.
    Am J Med Genet; 1989 Dec 12; 34(4):470-4. PubMed ID: 2624254
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  • 9. New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.
    Wilson M, Mulley J, Gedeon A, Robinson H, Turner G.
    Am J Med Genet; 1991 Sep 15; 40(4):406-13. PubMed ID: 1746601
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  • 10. A form of X-linked mental retardation with marfanoid habitus.
    Lujan JE, Carlin ME, Lubs HA.
    Am J Med Genet; 1984 Jan 15; 17(1):311-22. PubMed ID: 6711603
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  • 11. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
    Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1997 Dec 31; 73(4):474-9. PubMed ID: 9415477
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  • 12. Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome.
    Gedeon AK, Kozman HM, Robinson H, Pilia G, Schlessinger D, Turner G, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):63-8. PubMed ID: 8826450
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  • 14. X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large family.
    Gendrot C, Ronce N, Raynaud M, Ayrault AD, Dourlens J, Castelnau P, Muh JP, Chelly J, Moraine C.
    Am J Med Genet; 1999 Apr 23; 83(5):411-8. PubMed ID: 10232754
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  • 15. Nonspecific X-linked mental retardation with macrocephaly and obesity: a further family.
    Baraitser M, Reardon W, Vijeratnam S.
    Am J Med Genet; 1995 Jul 03; 57(3):380-4. PubMed ID: 7677138
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  • 16. Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31.
    Shrimpton AE, Daly KM, Hoo JJ.
    Am J Med Genet; 1999 May 28; 84(3):293-9. PubMed ID: 10331611
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  • 17. Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20).
    Lazzarini A, Stenroos ES, Lehner T, McKoy V, Gold B, McCormack MK, Reid CS, Ott J, Johnson WG.
    Am J Med Genet; 1995 Jul 17; 57(4):552-7. PubMed ID: 7573127
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  • 18. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.
    Am J Med Genet; 1999 Jul 30; 85(3):216-20. PubMed ID: 10398231
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  • 19. Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38).
    Schutz CK, Ives EJ, Chalifoux M, MacLaren L, Farrell S, Robinson PD, White BN, Holden JJ.
    Am J Med Genet; 1996 Jul 12; 64(1):89-96. PubMed ID: 8826457
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  • 20. A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region.
    Hamel BC, Wesseling P, Renier WO, van den Helm B, Ropers HH, Kremer H, Mariman EC.
    J Med Genet; 1999 Feb 12; 36(2):140-3. PubMed ID: 10051014
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