Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("G22)")

Filter

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 1735

  • Page / 70
Export

Selection :

  • and

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

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

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

CONTRIBUTO ALLA PATOLOGIA DEL CROMOSOMA 22. = CONTRIBUTION A LA PATHOLOGIE DU CHROMOSOME 22GIORDANO A; GRIMOLDI MG; LAVEZZI AM et al.1976; FOLIA HERED. PATHOL.; ITAL.; DA. 1976; VOL. 25; NO 2; PP. 38-52; ABS. ANGL.; BIBL. 1 P. 1/2Article

COMPLEX CHROMOSOMAL REARRANGEMENT LEADING TO PARTIAL TRISOMY 22HANSTEEN IL; SCHIRMER L; HESTETUN S et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 1; PP. 66-68; BIBL. 7 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

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

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

Report of the third international workshop on human chromosome 22 mappingEMANUEL, B. S; BUETOW, K; NUSSBAUM, R et al.Cytogenetics and cell genetics. 1993, Vol 63, Num 4, pp 206-211, issn 0301-0171Article

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

PARTIAL TRISOMY 22: A RECOGNIZABLE SYNDROME.GARLINGER P; MCGEARY SA; MAGENIS E et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 1; PP. 9-16; BIBL. 19 REF.Article

THE PROBLEM OF PARTIAL TRISOMY 22 RECONSIDEREDFELDMAN GM; SPARKES RS.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 1; PP. 97-101; BIBL. 10 REF.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

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

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

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

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

Assignment of the gene (UQCRFS1) for the Rieske iron-sulfur protein subunit of the mitochondrial cytochrome bc1 complex to the 22q13 and 19q12-q13.1 regions of the human genomeDUNCAN, A. M. V; ANDERSON, L; DUFF, C et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 281-283, issn 0888-7543Article

Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22MACOLLIN, M; PETERFREUND, R; MACDONALD, M et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 2, pp 332-333, issn 0888-7543Article

RFLP identified by the anonymous DNA segment FZ VI A2 at 22q11.2 [HGM no. D22A20]FANGRONG ZHANG; MONPEZAT, J.-P; DELATTRE, O et al.Nucleic acids research. 1988, Vol 16, Num 6, issn 0305-1048, 2739Article

Molecular genetic approach to human meningioma: loss of genes on chromosome 22SEIZINGER, B. R; DE LA MONTE, S; ATKINS, L et al.Proceedings of the National Academy of Sciences of the United States of America. 1987, Vol 84, Num 15, pp 5419-5423, issn 0027-8424Article

TRISOMIE 22 PARTIELLE.TAILLEMITE JL; BAHEUX MORLIER G; VAN DEN AKKER J et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 291-293; ABS. ANGL.; BIBL. 15 REF.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

  • Page / 70