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kw.\*:("Abnormal chromosome G21")

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Prenatal diagnosis of mosaic tetrasomy 21q confirmed by fluorescence in situ hybridizationNAGARSHETH, N. P; MOOTABAR, H.Clinical genetics. 1997, Vol 51, Num 4, pp 260-263, issn 0009-9163Article

Patient with a deletion of chromosome 21q and minimal phenotypeTINKEL-VERNON, Hilary; FINKERNAGEL, Scott; DESPOSITO, Franklin et al.American journal of medical genetics. 2003, Vol 120A, Num 1, pp 142-143, issn 0148-7299, 2 p.Article

Decreased resting metabolic rate among persons with Down syndromeALLISON, D. B; GOMEZ, J. E; HESHKA, S et al.International journal of obesity. 1995, Vol 19, Num 12, pp 858-861, issn 0307-0565Article

Unique mosaicism of structural chromosomal rearrangement: Is chromosome 18 preferentially involved?DE PATER, J. M; SMEETS, D. F. C. M; SCHERES, J. M. J. C et al.American journal of medical genetics. 2003, Vol 119A, Num 1, pp 26-31, issn 0148-7299, 6 p.Article

CARTOGRAPHIE PHYSIQUE ET TRANSCRIPTIONNELLE DE LA REGION CHROMOSOMIQUE 1 DE LA MONOSOMIE 21 CLONAGE ET CARACTERISATION DU GENE C21ORF6 = PHYSICAL AND TRANSCRIPTIONAL MAPPING OF THE MONOSOMY 21 CHROMOSOMAL REGION-1. CLONING AND CARACTERISATION OF THE C21ORF6 GENEOrti, Robert; Delabar, Jean.2000, 163 p.Thesis

An unbalanced translocation 46,XX, +der(18)t(18;21)(q12.2;q11.2)mat, -21 associated with maternal isodisomy 18pter→18q12.2DE RAVEL, Thomy J. L; MATTHIJS, Gert; FRYNS, Jean-Pierre et al.Annales de génétique (Paris). 2001, Vol 44, Num 2, pp 63-66, issn 0003-3995Article

Isodicentric chromosome 21 : A novel aberration in acute myeloid leukemiaSANKAR, M; TANAKA, K; ARIF, M et al.Cancer genetics and cytogenetics. 1998, Vol 107, Num 1, pp 69-72, issn 0165-4608Article

PRMT1 interacts with AML1-ETO to promote its transcriptional activation and progenitor cell proliferative potentialSHIA, Wei-Jong; OKUMURA, Akiko J; ZHANG, Dong-Er et al.Blood. 2012, Vol 119, Num 21, pp 4953-4962, issn 0006-4971, 10 p.Article

Nuchal translucency cannot be used as a screening test for chromosomal abnormalities in the first trimester of pregnancy in a routine ultrasound practiceKORNMAN, L. H; MORSSINK, L. P; BEEKHUIS, J. R et al.Prenatal diagnosis. 1996, Vol 16, Num 9, pp 797-805, issn 0197-3851Article

Persistence of AML1 rearrangement in peripheral blooc cells in t(8;21)KWONG, Y. L; WONG, K. F; CHAN, V et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 2, pp 151-154, issn 0165-4608Article

Down's syndrome with transient myeloproliferative disorderDHADED, S. M; DAS, R; KUMAR, P et al.Indian pediatrics. 1996, Vol 33, Num 11, pp 964-966, issn 0019-6061Article

Blood consult: acute myeloid leukemia and the t(8;21)(q22;22)PARK, Jae H; HEDVAT, Cyrus V; TALLMAN, Martin S et al.Blood. 2011, Vol 117, Num 10, pp 2775-2777, issn 0006-4971, 3 p.Article

Structure of the AML1-ETO eTAFH domain-HEB peptide complex and its contribution to AML1-ETO activityPARK, Sangho; WEI CHEN; CIERPICKI, Tomasz et al.Blood. 2009, Vol 113, Num 15, pp 3558-3567, issn 0006-4971, 10 p.Article

Ring chromosome 21 in a boy and a derivative chromosome 21 in the mother: Implication for ring chromosome formationMUROYA, Koji; YAMAMOTO, Keiichi; FUKUSHIMA, Yoshimitsu et al.American journal of medical genetics. 2002, Vol 110, Num 4, pp 332-337, issn 0148-7299Article

Partial 1q and 21p trisomies in a male child due to maternal t (1; 21)RAJANGAM, S; LINCOLN, S; HEGDE, S et al.Indian journal of pediatrics. 1999, Vol 66, Num 2, pp 301-303, issn 0019-5456Article

A jumping Robertsonian translocation : a molecular and cytogenetic studyGROSS, S. J; THARAPEL, A. T; PHILLIPS, O. P et al.Human genetics. 1996, Vol 98, Num 3, pp 291-296, issn 0340-6717Article

Down syndrome with partial duplication and del (21) syndrome : study protocol and call for collaboration. Study I: clinical assessmentBARNICOAT, A. J; BONNEAU, J. L; SHAFEI-BENAISSA, E et al.Clinical genetics. 1996, Vol 49, Num 1, pp 20-27, issn 0009-9163Article

De novo balanced 5;21 translocation in a child with acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardationHORDNES, K; ENGEBRETSEN, L. F; KNUDTZON, J et al.Clinical genetics. 1995, Vol 48, Num 6, pp 321-323, issn 0009-9163Article

Physical findings in 21q22 deletion suggest critical region for 21q-phenotype in q22THEODOROPOULOS, D. S; COWAN, J. M; ELIAS, E. R et al.American journal of medical genetics. 1995, Vol 59, Num 2, pp 161-163, issn 0148-7299Article

Aleukaemic acute myeloid leukaemia with t(8;21)(q22;q22)WONG, K. F; SIU, Lisa L. P; WONG, W. S et al.British journal of haematology. 2009, Vol 146, Num 4, issn 0007-1048, p. 345Article

Identification of AML1-ETO modulators by chemical genomicsCORSELLO, Steven M; ROTI, Giovanni; ROSS, Kenneth N et al.Blood. 2009, Vol 113, Num 24, pp 6193-6205, issn 0006-4971, 13 p.Article

Aberrant transcriptional regulation of the MLL fusion partner EEN by AML1-ETO and its implication in leukemogenesisMA, Li-Heng; HAN LIU; ZHU CHEN et al.Blood. 2007, Vol 109, Num 2, pp 769-777, issn 0006-4971, 9 p.Article

A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridizationFLAHERTY, L; MOLONEY, J; WATSON, N et al.JIDR. Journal of intellectual disability research (Print). 1998, Vol 42, Num 3, pp 254-258, issn 0964-2633Article

Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridizationBLANCO, J; EOGZCUE, J; VIDAL, F et al.Human reproduction (Oxford. Print). 1996, Vol 11, Num 4, pp 722-726, issn 0268-1161Article

Myelodysplasia in childhood may be a polyclonal diseaseTCHERNIA, G; BADER-MEUNIER, B; LAVERGNE, J. M et al.Hematology and cell therapy (Print). 1996, Vol 38, Num 4, pp 325-330, issn 1269-3286Article

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