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

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

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

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 CASE OF "G2 DELATION SYNDROME" RING OR PARTIAL MONOSOMY. (46, XX, 22R OR 46, XX, 22P..).MILANI COMPARETTI M; ROSSOLINI V; PACE DP et al.1975; ACTA GENET. AND GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 3-4; PP. 311-313; BIBL. 5 REF.Article

AN R(22) (P11->Q13) IN A MODERATELY MENTALLY RETARDED GIRLALLER V; ABRISQUETA JA; DE TORRES ML et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 157-162; BIBL. 18 REF.Article

FOUR NEW CASES OF RING 21 AND 22 INCLUDING FAMILIAL TRANSMISSION OF RING 21.PALMER CG; HODES ME; REED T et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 1; PP. 54-60; BIBL. 1 P.Article

LE SYNDROME II DE DELETION G. A PROPOS D'UNE OBSERVATION DE CHROMOSOME 22 EN ANNEAU.MALLARD BENE M.1976; ; S.L.; DA. 1976; PP. 1-103; H.T. 17; BIBL. 17 P. 1/2; (THESE DOCT. MED.; DIJON)Thesis

LE SYNDROME R(22). APGPOS DE 4 NOUVELLES OBSERVATIONS.RETHORE MO; NOEL B; COUTURIER J et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 2; PP. 111-117; ABS. ANGL.; BIBL. 13 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

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

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

CHROMOSOMAL MAPPING OF THE SIMIAN SARCOMA VIRUS ONC GENE ANALOGUE IN HUMAN CELLSSWAN DC; MCBRIDE OW; ROBBINS KC et al.1982; PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. BIOLOGICAL SCIENCES; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 15; PP. 4691-4695; BIBL. 50 REF.Article

IDENTIFICATION BY FLUORESCENCE OF TWO G RINGS: (46XY, 21R) G DELETION SYNDROME I AND (46, XX, 22R) G DELETION SYNDROME IIMAGENIS RE; ARMENDARES S; HECHT F et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 265-266; ABS. FR.Serial Issue

PHILADELPHIA CHROMOSOME WITH T(6;22) (P25;Q12)MAMMON Z; GRINBLAT J; JOSHUA H et al.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 294; NO 16; PP. 827-828; BIBL. 8 REF.Article

MONOZYGOTIC TWINS WITH RING CHROMOSOME 22 = JUMEAUX MONOZYGOTES PORTEURS D'UN CHROMOSOME 22 ANNULAIRELINDENBAUM RH; BOBROW M; BARBER L et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 1; PP. 85-89; BIBL. 26 REF.Serial Issue

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

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

UNEXPECTED FINDINGS WITH THE NEW CHROMOSOME BANDING TECHNIQUES IN A PATIENT FORMERLY DIAGNOSED AS HAVING G-DELETION SYNDROME = RESULTATS INATTENDUS OBTENUS GRACE AUX NOUVELLES TECHNIQUES DE BANDES CHEZ UNE PATIENTE DIAGNOSTIQUEE INITIALEMENT COMME ATTEINTE DE SYNDROME II DE DELETION GORYE E; CRAEN M.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 75-82; ABS. ITAL. FR. ALLEM.; BIBL. 14 REF.Article