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| Title : X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family - Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| Author(s) : Laumonnier F , Bonnet-Brilhault F , Gomot M , Blanc R , David A , Moizard MP , Raynaud M , Ronce N , Lemonnier E , Calvas P , Laudier B , Chelly J , Fryns JP , Ropers HH , Hamel BC , Andres C , Barthelemy C , Moraine C , Briault S |
| Ref : American Journal of Human Genetics , 74 :552 , 2004 |
| Abstract : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| ESTHER : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| PubMedSearch : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| PubMedID: 14963808 |
| Gene_locus related to this paper: human-NLGN4X |
| Title : Evidence against a major role of PEG1\/MEST in Silver-Russell syndrome - Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| Author(s) : Riesewijk AM , Blagitko N , Schinzel AA , Hu L , Schulz U , Hamel BC , Ropers HH , Kalscheuer VM |
| Ref : Eur J Hum Genet , 6 :114 , 1998 |
| Abstract : Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| ESTHER : Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| PubMedSearch : Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| PubMedID: 9781054 |
| Title : Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation - Kotzot_1995_Hum.Mol.Genet_4_583 |
| Author(s) : Kotzot D , Schmitt S , Bernasconi F , Robinson WP , Lurie IW , Ilyina H , Mehes K , Hamel BC , Otten BJ , Hergersberg M , Werder E , Schoenle E , Schinzel A |
| Ref : Hum Mol Genet , 4 :583 , 1995 |
| Abstract : Kotzot_1995_Hum.Mol.Genet_4_583 |
| ESTHER : Kotzot_1995_Hum.Mol.Genet_4_583 |
| PubMedSearch : Kotzot_1995_Hum.Mol.Genet_4_583 |
| PubMedID: 7633407 |