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A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22PARRUTI, G; DI ILIO, C; CALABRESE, G et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 55-58, issn 0003-3995, 4 p.Article

Interstitial deletion of 2 (q33q36) in a child with congenital abnormalitiesGORSKI, J. L; KIYNE, M; UHLMANN, W et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 204-205, issn 0022-2593, 2 p.Article

Response by Dr. WassmanWASSMAN, E. R.American journal of medical genetics. 1988, Vol 29, Num 2, pp 455-456, issn 0148-7299Article

Clinical phenotype associated with terminal 2q37 deletionCONRAD, B; DEWALD, G; CHRISTENSEN, E et al.Clinical genetics. 1995, Vol 48, Num 3, pp 134-139, issn 0009-9163Article

Interstitial deletion 2q34.3: case report with high resolution bandingBERNAR, J; SPARKES, R. S; ALLENSWORTH, S et al.Journal of medical genetics. 1985, Vol 22, Num 3, pp 226-228, issn 0022-2593Article

Del(2)(p23) : a new recurrent abnormality in acute myeloid leukemiaNAJFELD, V; SCALISE, A; FRUCHTMAN, S et al.Cancer genetics and cytogenetics. 1990, Vol 46, Num 2, pp 185-190, issn 0165-4608, 6 p.Article

A new case of familial paracentric inversion of chromosome 2DONTI, E; ROSETTI, A; CARLONI, I et al.Human genetics. 1987, Vol 75, Num 2, issn 0340-6717, 195Article

Deletion 2q syndrome?SANCHEZ, J. M.American journal of medical genetics. 1988, Vol 29, Num 2, pp 453-454, issn 0148-7299Article

Is the expression of fra (2) (q13) age dependent?FRYNS, J. P; VAN DEN BERGHE, H.Journal of medical genetics. 1988, Vol 25, Num 10, issn 0022-2593, 718 [1 p.]Article

Deletion (2)(q37)STRATTON, R. F; TOLWORTHY, J. A; YOUNG, R. S et al.American journal of medical genetics. 1994, Vol 51, Num 2, pp 153-155, issn 0148-7299Article

Chromosome 5 aberrations and genetic predisposition to lung cancerWU, X; ZHAO, Y; KEMP, B. L et al.International journal of cancer. 1998, Vol 79, Num 5, pp 490-493, issn 0020-7136Article

Interstitial deletion 2P accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosomePETIT, P; FRYNS, J. P.Genetic counseling. 1997, Vol 8, Num 4, pp 341-343, issn 1015-8146Conference Paper

A region-specific microdissection library for human chromosome 2p23-p25 and the analysis of an interstitial deletion of 2p23.3-p25.1JINGWEI YU; JIANXI QI; SUHONG TONG et al.Human genetics. 1994, Vol 93, Num 5, pp 557-562, issn 0340-6717Article

Del(2q) : cause of the wrinkly skin syndrome ?KREUZ, F. R; WITTWER, B. H.Clinical genetics. 1993, Vol 43, Num 3, pp 132-138, issn 0009-9163Article

t(2;3)(p13;q26) in a case of chronis myeloid leukemia : importance of the involvement of 3q26KWONG, Y. L; CHAN, L. C; LIE, K. W et al.Cancer genetics and cytogenetics. 1992, Vol 59, Num 1, pp 95-96, issn 0165-4608Article

Translocation (2;7) (pl3;q36) in a case of acute nonlymphocytic leukemia evolving from a myelodysplastic syndromeCHANDRIKA SREEKANTAIAH; BAER, M. R; SOLE, F et al.Cancer genetics and cytogenetics. 1988, Vol 35, Num 2, pp 199-204, issn 0165-4608Article

Brief clinical report: a patient with partial duplication 2q and partial deficiency 11qCHEN-KUNG HO; HENDERSON, K. C; BOWYER, F. P et al.American journal of medical genetics. 1987, Vol 28, Num 3, pp 575-579, issn 0148-7299Article

Deletion of 2p: a cytogenetic and clinical updateNEIDICH, J; ZACKAI, E; ARONSON, M et al.American journal of medical genetics. 1987, Vol 27, Num 3, pp 707-710, issn 0148-7299Article

Génétique des trisomies partielles. I. Trisomie 2qLUR'E, I. V; RUMYANTSEVA, N. V; PODLESHCHUK, L. V et al.Genetika. 1986, Vol 22, Num 6, pp 1033-1039, issn 0016-6758Article

The significance of pericentric inversions of chromosome 2DJALALI, M; STEINBACH, P; BULLERDIEK, J et al.Human genetics. 1986, Vol 72, Num 1, pp 32-36, issn 0340-6717Article

Familial paracentric inversion inv(2)(q31q36)SCHMID, M; HOFMANN, R; KÖHLER, J et al.Human genetics. 1985, Vol 71, Num 3, pp 270-272, issn 0340-6717Article

A specific chromosome aberration in a keratoacanthomaKIM, Dae-Kwang; KIM, Joo-Young; KIM, Hyeung-Tae et al.Cancer genetics and cytogenetics. 2003, Vol 142, Num 1, pp 70-72, issn 0165-4608, 3 p.Article

Chromosome 2q duplications : Case report of a de novo interstitial duplication and review of the literatureBIRD, Lynne M; MASCARELLO, James T.American journal of medical genetics. 2001, Vol 100, Num 1, pp 13-24, issn 0148-7299Article

Trisomy 2q11.2→q21,1 resulting from an unbalanced insertion in two generationsGLASS, I. A; STORMER, P; OEI, P. T. S. P et al.Journal of medical genetics. 1998, Vol 35, Num 4, pp 319-322, issn 0022-2593Article

Interstitial deletion 2(p11.2p13) : a rare chromosomal abnormalityWENGER, S. L; MCPHERSON, E. W.Clinical genetics. 1997, Vol 52, Num 1, pp 61-62, issn 0009-9163Article

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