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Volumn 94, Issue 5, 2000, Pages 376-382

Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: Linkage analysis and clinical findings in a three-generation Sardinian family

(8) Russo, S a Cogliati, F a Cavalleri, F a Cassitto, M G b Giglioli, R b Toniolo, D c Casari, G d Larizza, L a,b

a ISTITUTO AUXOLOGICO ITALIANO (Italy)

b UNIVERSITY OF MILAN (Italy)

c CNR (Italy)

d TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM (Italy)

Author keywords

MRX72; X linked non specific mental retardation; Xq28 mapping

Indexed keywords

ARTICLE; CHROMOSOME XQ; CLINICAL ARTICLE; FEMALE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENETIC MARKER; GENETIC RECOMBINATION; HUMAN; MALE; MENTAL DEFICIENCY; MOLECULAR CLONING; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; X CHROMOSOME RECESSIVE DISORDER;

ADOLESCENT; ADULT; CHILD; CHROMOSOME MAPPING; DNA; FAMILY HEALTH; FEMALE; HUMANS; ITALY; LINKAGE (GENETICS); LOD SCORE; MALE; MENTAL RETARDATION; MICROSATELLITE REPEATS; MIDDLE AGED; PEDIGREE; X CHROMOSOME;

EID: 0034706405 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(20001023)94:5<376::AID-AJMG6>3.0.CO;2-A Document Type: Article

Times cited : (11)

References (22)

1
- 0031710557
- PAK3 mutation in nonsyndromic X-linked mental retardation
- (1998) Nat Genet , vol.20 , pp. 25-30
- Allen, K.M.¹ Gleeson, J.G.² Bagrodia, S.³ Pantington, M.W.⁴ MacMillan, J.C.⁵ Cerione, R.A.⁶ Mulley, J.⁷ Walsh, C.A.⁸

2
- 0031865393
- Mind the GAP, Rho, Rab and GDI
- (1998) Nature , vol.19 , pp. 106-108
- Antonarakis, S.E.¹ Aelst, L.V.²

3
- 7344219887
- Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor
- (1998) , vol.7 , pp. 1311-1315
- Bienvenu, T.¹ Des Portes, V.² Martin, A.S.³ McDonell, N.⁴ Billuart, P.⁵ Carrie, A.⁶ Vinet, M.C.⁷ Couvert, P.⁸ Toniolo, D.⁹ Ropers, H.H.¹⁰ Moraine, C.¹¹ Van Bokhoven, H.¹² Fryns, J.P.¹³ Kahn, A.¹⁴ Beldjord, C.¹⁵ Chelly, J.¹⁶

4
- 0032580161
- Oligophrenin-1 encodes a pGAP protein involved in X-linked mental retardation
- (1998) Nature , vol.392 , pp. 823-826
- Billuart, P.¹ Bienvenu, T.² Ronce, N.³ Des Pontes, V.⁴ Vinet, M.C.⁵ Zemni, R.⁶ Crollius, H.R.⁷ Carrie, A.⁸ Fauchereau, F.⁹ Cherry, M.¹⁰ Briault, S.¹¹ Hamel, B.¹² Fryns, J.P.¹³ Beldjord, C.¹⁴ Kahn, A.¹⁵ Moraine, C.¹⁶ Chelly, J.¹⁷

5
- 0032819848
- A new member of IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
- (1999) Nat Genet , vol.23 , pp. 25-31
- Carrie, A.¹ Jun, L.² Bienvenu, T.³ Vinet, M.C.⁴ McDonell, N.⁵ Couvert, P.⁶ Zemni, R.⁷ Cardona, A.⁸ Van Buggenhout, G.⁹ Frints, S.¹⁰ Hamel, B.¹¹ Moraine, C.¹² Ropers, H.H.¹³ Strom, T.¹⁴ Howell, G.R.¹⁵ Whittaker, A.¹⁶ Ross, M.T.¹⁷ Kahn, A.¹⁸ Fryns, J.P.¹⁹ Beldjord, C.²⁰ Marynen, P.²¹ Chelly, J.²² more..

6
- 17344369362
- Mutations in GDI1 are responsible for X-linked mental retardation
- (1998) Nat Genet , vol.19 , pp. 134-139
- D'Adamo, P.¹ Menegon, A.² Lo Nigro, C.³ Grasso, M.⁴ Gulisano, M.⁵ Tamarini, F.⁶ Bienvenu, T.⁷ Gedeon, A.K.⁸ Oostra, B.⁹ Wu, S.K.¹⁰ Tandon, A.¹¹ Valtorta, F.¹² Balch, W.E.¹³ Chelly, J.¹⁴ Toniolo, D.¹⁵

7
- 16944364477
- A gene for dominant nonspecific X-linked mental retardation is located in Xq28
- (1997) Am J Hum Genet , vol.60 , pp. 903-909
- Des Pontes, V.¹ Billuart, P.² Carrie, A.³ Bachner, L.⁴ Bienvenu, T.⁵ Vinet, M.C.⁶ Beldjord, C.⁷ Ponsot, G.⁸ Kahn, A.⁹ Boue, J.¹⁰ Chelly, J.¹¹

8
- 13344259999
- A comprehensive genetic map of the human genome based on 5,264 microsatellites
- (1996) Nature , vol.380 , pp. 152-154
- Dib, C.¹ Faure, S.² Fizames, C.³ Samson, D.⁴ Drouot, N.⁵ Vignal, A.⁶ Millasseau, P.⁷ Millasseau, P.⁸ Marc, S.⁹ Hazan, J.¹⁰ Seboun, E.¹¹ Lathrop, M.¹² Gyapay, G.¹³ Morissette, J.¹⁴ Weissenbach, J.¹⁵

9
- 0030137717
- Identification of the gene FMR2, associated with FRAXE mental retardation
- (1996) Nat Genet , vol.13 , pp. 105-108
- Gecz, J.¹ Gedeon, A.K.² Sutherland, G.R.³ Mulley, J.C.⁴

10
- 0025884456
- Localization of the MRX3 gene for non-specific X-linked mental retardation (MRX)
- (1991) J Med Genet , vol.28 , pp. 372-377
- Gedeon, A.¹ Mulley, J.² Turner, G.³

11
- 0033597287
- X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28
- (1999) Am J Med Genet , vol.83 , pp. 411-418
- Gendrot, C.¹ Ronce, N.² Raynaud, M.³ Ayrault, A.D.⁴ Dourlens, J.⁵ Castelnau, P.⁶ Muh, J.-P.⁷ Chelly, J.⁸ Moraine, C.⁹

12
- 0029949944
- A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28
- (1996) Am J Med Genet , vol.64 , pp. 131-133
- Hamel, B.J.C.¹ Kremer, H.² Wesby-Van Swaay, E.³ Van del Helm, B.⁴ Smits, A.P.T.⁵ Oostra, B.A.⁶ Ropers, H.H.⁷ Mariman, E.M.C.⁸

13
- 0029950258
- Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)
- (1996) Am J Med Genet , vol.64 , pp. 125-130
- Holinski-Feder, E.¹ Golla, A.² Rost, I.³ Seidel, H.⁴ Rittinger, O.⁵ Meindl, A.⁶

14
- 0027203684
- Trinucleotide repeat amplification and hypermethylation of CpG island in FRAXE mental retardation
- (1993) Cell , vol.74 , pp. 127-134
- Knight, S.J.L.¹ Flannery, A.V.² Hirst, M.C.³ Campbell, L.⁴ Christodoulou, Z.⁵ Phelps, S.R.⁶ Pointon, J.⁷ Middleton-Price, H.R.⁸ Barnicoat, A.⁹ Pembrey, M.E.¹⁰ Hollan, J.¹¹ Oostra, B.A.¹² Bobrow, M.¹³ Davies, K.E.¹⁴

15
- 0002554724
- A new form of X-linked mental retardation (XLMR) linked to DXS369 (RN1)
- (1991) Cytogenet Cell Genet , vol.58 , pp. 2071
- Kondo, I.¹ Tsukamoto, K.² Niikawa, N.³ Okano, K.⁴ Kanazawa, I.⁵ Hupkes, P.E.⁶

16
- 0342499587
- Strategies for multilocus linkage analysis in humans
- (1984) Proc Nat Acad Sci USA , vol.81 , pp. 3443-3446
- Lathrop, G.M.¹ Lalouel, J.M.² Julier, C.³ Ott, J.⁴

17
- 0033515499
- XLMR Genes: Update 1998
- (1999) Am J Med Genet , vol.83 , pp. 237-247
- Lubs, H.¹ Chiurazzi, P.² Arena, J.³ Schwartz, C.⁴ Tranebjaerg, L.⁵ Neri, G.⁶

18
- 0027486670
- Evidence that methylation of the FMR-1 locus is responsible for variable phenotypic expression of the fragile X syndrome
- (1993) Am J Hum Genet , vol.53 , pp. 800-809
- McConkie-Rosell, A.¹ Lachiewics, A.M.² Spiridigliozzi, G.A.³ Tarleton, J.⁴ Schoenwald, S.⁵ Phelan, M.C.⁶ Goonewardena, P.⁷ Ding, X.⁸ Brown, W.T.⁹

19
- 0032910443
- A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation
- (1999) Nat Genet , vol.22 , pp. 13-14
- Merienne, K.¹ Jacquot, S.² Pannetier, S.³ Zeniou, M.⁴ Bankier, A.⁵ Gecz, J.⁶ Mandel, J.L.⁷ Mulley, J.⁸ Sassone-Corsi, P.⁹ Hanauer, A.¹⁰

20
- 0026526250
- Linkage to Xq28 in a family with non-specific X-linked mental retardation
- (1992) Hum Genet , vol.90 , pp. 263-266
- Nordstrom, A.M.¹ Penttinen, M.² Von Koskull, H.³

21
- 0026339303
- Instability of 550 base pair DNA segment and abnormal methylation in fragile X syndrome
- (1991) Science , vol.252 , pp. 1098-1102
- Oberle, I.¹ Rosseau, F.² Heitz, D.³ Devyis, D.⁴ Hanauer, A.⁵ Boue, J.⁶ Bertheas, M.F.⁷ Mandel, J.L.⁸

22
- 0030875988
- A new X-linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28
- (1997) J Med Genet , vol.34 , pp. 529-534
- Pai, S.G.¹ Hane, B.² Joseph, M.³ Nelson, R.⁴ Hammond, L.S.⁵ Arena, J.F.⁶ Lubs, H.A.⁷ Stevenson, R.E.⁸ Schwartz, C.E.⁹

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