Increase in serum concentrations of IgG2 and IgG4 by selenium supplementation in children with Down's syndrome.

Por Annerén, G, Magnusson, C G, Nordvall, S L
Publicado em 1990

Growth charts for Down's syndrome from birth to 18 years of age

Por Myrelid, A, Gustafsson, J, Ollars, B, Anneren, G
Publicado em 2002

Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis.

Por Wadelius, C, Fagerholm, P, Pettersson, U, Annerén, G
Publicado em 1989

Growth and somatomedin responses to growth hormone in Down's syndrome.

Por Annerén, G, Sara, V R, Hall, K, Tuvemo, T
Publicado em 1986

Abnormal interferon production and NK cell responses to interferon in children with Down's syndrome

Por Funa, Keiko, Annerén, G., Alm, G. V., Björkstén, B.
Publicado em 1984

Thyroid dysfunction in Down's syndrome: relation to age and thyroid autoimmunity

Por Karlsson, B, Gustafsson, J, Hedov, G, Ivarsson, S, Anneren, G
Publicado em 1998

Abnormal serum IgG subclass pattern in children with Down's syndrome.

Por Annerén, G, Magnusson, C G, Lilja, G, Nordvall, S L
Publicado em 1992

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Por Blennow, E, Annerén, G, Bui, T H, Berggren, E, Asadi, E, Nordenskjöld, M
Publicado em 1993

Growth hormone treatment in young children with Down's syndrome: effects on growth and psychomotor development

Por Anneren, G, Tuvemo, T, Carlsson-Skwirut, C, Lonnerholm, T, Bang, P, Sara, V, Gustafsson, J
Publicado em 1999

Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene

Por Dianzani, I, Garelli, E, Gustavsson, P, Carando, A, Gustafsson, B, Dahl, N, Anneren, G
Publicado em 2003

Interstitial Deletions at 6q14.1–q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype

Por Wentzel, C., Lynch, S.A., Stattin, E.-L., Sharkey, F.H., Annerén, G., Thuresson, A.-C.
Publicado em 2010

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

Por Thuresson, A.-C., Bondeson, M.-L., Edeby, C., Ellis, P., Langford, C., Dumanski, J.P., Annerén, G.
Publicado em 2007

Linkage mapping of a severe X-linked mental retardation syndrome.

Por Malmgren, H, Sundvall, M, Dahl, N, Gustavson, K H, Annerén, G, Wadelius, C, Steén-Bondeson, M L, Pettersson, U
Publicado em 1993

Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).

Por Dahl, N, Goonewardena, P, Malmgren, H, Gustavson, K H, Holmgren, G, Seemanova, E, Annerén, G, Flood, A, Pettersson, U
Publicado em 1989

An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

Por Annerén, G, Andersson, M, Page, D C, Brown, L G, Berg, M, Läckgren, G, Gustavson, K H, de la Chapelle, A
Publicado em 1987

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.

Por Arnell, H, Hjälmås, K, Jägervall, M, Läckgren, G, Stenberg, A, Bengtsson, B, Wassén, C, Emahazion, T, Annerén, G, Pettersson, U, Sundvall, M, Dahl, N
Publicado em 1997

Protocols to establish genotype-phenotype correlations in Down syndrome.

Por Epstein, C J, Korenberg, J R, Annerén, G, Antonarakis, S E, Aymé, S, Courchesne, E, Epstein, L B, Fowler, A, Groner, Y, Huret, J L
Publicado em 1991

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

Por Shah, A B, Chernov, I, Zhang, H T, Ross, B M, Das, K, Lutsenko, S, Parano, E, Pavone, L, Evgrafov, O, Ivanova-Smolenskaya, I A, Annerén, G, Westermark, K, Urrutia, F H, Penchaszadeh, G K, Sternlieb, I, Scheinberg, I H, Gilliam, T C, Petrukhin, K
Publicado em 1997

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

Por Molin, A-M, Andrieux, J, Koolen, D A, Malan, V, Carella, M, Colleaux, L, Cormier-Daire, V, David, A, de Leeuw, N, Delobel, B, Duban-Bedu, B, Fischetto, R, Flinter, F, Kjaergaard, S, Kok, F, Krepischi, A C, Le Caignec, C, Ogilvie, C Mackie, Maia, S, Mathieu-Dramard, M, Munnich, A, Palumbo, O, Papadia, F, Pfundt, R, Reardon, W, Receveur, A, Rio, M, Ronsbro Darling, L, Rosenberg, C, Sá, J, Vallee, L, Vincent-Delorme, C, Zelante, L, Bondeson, M-L, Annerén, G
Publicado em 2011

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Por Hu, H, Haas, S A, Chelly, J, Van Esch, H, Raynaud, M, de Brouwer, A P M, Weinert, S, Froyen, G, Frints, S G M, Laumonnier, F, Zemojtel, T, Love, M I, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K L, Belet, S, van Roozendaal, K E P, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L B, Wieacker, P, Rodríguez Criado, G, Bondeson, M-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T J, Chen, W, Ropers, H-H, Kalscheuer, V M
Publicado no Mol Psychiatry (2016)