Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Cromosoma 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 2276

  • Page / 92
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

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

The gene encoding the large human neurofilament subunit (NF-H) maps to the q121-q131 region on human chromosome 22MATTEI, M.-G; DAUTIGNY, A; PHAM-DINH, D et al.Human genetics. 1988, Vol 80, Num 3, pp 293-295, issn 0340-6717Article

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

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

The locus positioning problemEDWARDS, J. H.Annals of human genetics. 1989, Vol 53, pp 271-275, issn 0003-4800, 3Article

A linkage and physical map of chromosome 22, and some applications to gene mappingJULIER, C; LATHROP, G. M; REGHIS, A et al.American journal of human genetics. 1988, Vol 42, Num 2, pp 297-308, issn 0002-9297Article

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

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

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

Two members of the S-lac lectin gene family, LGALS1 and LGALS2, reside in close proximity on human chromosome 22q12-q13MEHRABIAN, M; GITT, M. A; SPARKES, R. S et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 2, pp 418-420, issn 0888-7543Article

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1→q11.2GROSSMAN, M. H; EMANUEL, B. S; BUDARF, M. L et al.Genomics (San Diego, Calif.). 1992, Vol 12, Num 4, pp 822-825, issn 0888-7543Article

Localization of the βA4-crystallin gene (CRYBA4) on human chromosome 22 in the region q11.2→q13.1VAN RENS, G. L. M; GEURTS VAN KESSELK, A. H. M; BLOEMENDAL, H et al.Cytogenetics and cell genetics. 1992, Vol 61, Num 3, pp 180-183, issn 0301-0171Article

  • Page / 92