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Unusual Four-Generation Chromosome-22 Rearrangement: When Normality Masks AbnormalityNEVADO, Julian; DE TORRES, M. Luisa; LAPUNZINA, Pablo et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1561-1564, issn 1552-4825, 4 p.Article

Tracheobronchial anomalies in chromosome 22q11.2 microdeletionBERTOLANI, Maria Francesca; BERGAMINI, Barbara Maria; PREDIERI, Barbara et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 7, pp 790-793, issn 1552-4825, 4 p.Article

The characteristics of human genes: analysis of human chromosome 22 : Functional Genomics and Disease 2003DUNHAM, Ian; BEARE, David M; COLLINS, John E et al.Comparative and functional genomics. 2003, Vol 4, Num 6, pp 635-646, issn 1531-6912, 12 p.Conference Paper

Microduplication and triplication of 22q11.2 : A highly variable syndromeYOBB, Twila M; SOMERVILLE, Martin J; CHERNOS, Judy et al.American journal of human genetics. 2005, Vol 76, Num 5, pp 865-876, issn 0002-9297, 12 p.Article

A NOTE ON A PATIENT WITH A RING-22 CHROMOSOME IDENTIFIED BY BANDINGSTEWART A; RICHARDS BW.1976; J. MENTAL DEFIC. RES.; G.B.; DA. 1976; VOL. 20; NO 2; PP. 95-98; BIBL. 2 REF.Article

Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2TSILCHOROZIDOU, T; MENKO, F. H; BROWN, A et al.Journal of medical genetics. 2004, Vol 41, Num 7, pp 529-534, issn 0022-2593, 6 p.Article

Defining the clinical spectrum of deletion 22q11.2ROBIN, Nathaniel H; SHPRINTZEN, Robert J.The Journal of pediatrics. 2005, Vol 147, Num 1, pp 90-96, issn 0022-3476, 7 p.Article

LA SINDROME R(22). = LE SYNDROME R(22)CURATOLO P; PAOLELLA A; PORRO G et al.1978; CLIN. PEDIATR.; ITAL.; DA. 1978; VOL. 60; NO 1; PP. 10-17; ABS. ANGL.; BIBL. 11 REF.Article

Five new subjects with ring chromosome 22ISHMAEL, H. A; CATALDI, D; BEGLEITER, M. L et al.Clinical genetics. 2003, Vol 63, Num 5, pp 410-414, issn 0009-9163, 5 p.Article

Bases moléculaires de la microdélétion 22q11 = Molecular basis of the microdeletion 22q11BOUVAGNET, P.Archives de pédiatrie (Paris). 2002, Vol 9, pp 97s-99s, issn 0929-693X, SUP2Conference Paper

Übermässiges Wachstum und Entwicklungsverzögerung assoziiert mit chromosomaler Deletion 22q13 = Overgrowth and retarded development associated with chromosome 22q13 deletionHINKEL, G. K; BARTSCH, O; BLIN, N et al.Monatsschrift für Kinderheilkunde. 1997, Vol 145, Num 9, pp 892-896, issn 0026-9298Conference Paper

FISH-mapping of a 100-kb terminal 22q13 deletionANDERLID, Britt-Marie; SCHOUMANS, Jacqueline; ANNEREN, Göran et al.Human genetics. 2002, Vol 110, Num 5, pp 439-443, issn 0340-6717Article

Synapsin III gene polymorphisms and schizophreniaOHMORI, O; SHINKAI, T; HORI, H et al.Neuroscience letters. 2000, Vol 279, Num 2, pp 125-127, issn 0304-3940Article

Comment on: Polymicrogyria versus pachygyria in 22q11 microdeletionDE WIT, Marie Claire Y; DE CON, René F. M; LEQUIN, Maarten H et al.American journal of medical genetics. 2005, Vol 136A, Num 4, pp 419-421, issn 0148-7299, 3 p.Article

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersDURAND, Christelle M; BETANCUR, Catalina; SPONHEIM, Eili et al.Nature genetics. 2007, Vol 39, Num 1, pp 25-27, issn 1061-4036, 3 p.Article

Assignment of AR1, transcription factor 20 (TCF20), to human chromosome 22q13.3 with somatic cell hybrids and in situ hybridizationRAJADHYAKSHA, A; RIVIERE, M; VAN VOOREN, P et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 3-4, pp 176-177, issn 0301-0171Conference Paper

Systematic evaluation of map quality: Human chromosome 22MATISE, Tara C; PORTER, Christopher J; BUYSKE, Steven et al.American journal of human genetics. 2002, Vol 70, Num 6, pp 1398-1410, issn 0002-9297Article

PHENOTYPIC CORRELATIONS IN PATIENTS WITH RING CHROMOSOME 22.HUNTER AGW; RAY M; WANG HS et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 4; PP. 239-249; BIBL. 26 REF.Article

VARIABILITY OF R(22) CHROMOSOME PHENOTYPICAL EXPRESSION.DALLAPICCOLA B; BRINCHI V; CURATOLO P et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 287-290; BIBL. 4 REF.Article

A CASE OF RING CHROMOSOME G22.BROOKFIELD DSK; WALKER S.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 530-532; BIBL. 6 REF.Article

CONTRIBUTION A L'ETUDE D'UN SYNDROME CLINIQUE ET CYTOGENETIQUE DE CHROMOSOME 22 EN ANNEAU: A PROPOS DE DEUX NOUVELLES OBSERVATIONSALLARD CHRISTIAN.1980; ; FRA; DA. 1980; 146; 102 P.: ILL.; 30 CM; BIBL. 94 REF.; TH.: MED./PARIS 5/1980Thesis

INDICATIONS FOR CHROMOSOME ANALYSIS ILLUSTRATED BY A CASE OF RING 22.HOWARD PEEBLES PN.1977; J. HERED.; U.S.A.; DA. 1977; VOL. 68; NO 4; PP. 268-269; BIBL. 11 REF.Article

PHENOTYPIC VARIATION IN TWO PATIENTS WITH A RING CHROMOSOME 22FUNDERBURK SJ; SPARKES RS; KLISAK I et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 5; PP. 305-310; BIBL. 23 REF.Article

Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndromeDE PIERO, A. D; LOURIE, E. M; BERMAN, B. W et al.The Journal of pediatrics. 1997, Vol 131, Num 3, pp 484-486, issn 0022-3476Article

Developmental aspects of 22q. 11 deletion syndromeArchives of disease in childhood. 2006, Vol 91, Num 4, pp 345-345, issn 0003-9888, 1 p.Article

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