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TERTIARY TRISOMY (22Q11Q),47,+DER(22), T(11;22)BIEDERMAN BM; LIN CC; LOWRY RB et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 173-177; BIBL. 34 REF.Article

PARTIAL TRISOMY OF 13 (PTER->Q12) DUE TO 47, XY,+DER (13), T(13; 22) (Q12; Q13)MATMOEDJONO SJ; SPARKES RS.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 241-246; BIBL. 19 REF.Article

PARTIAL TRISOMY 13. THE MYTH OF NONMONGOLOID TRISOMY GPATIL SR; ZELLWEGER H.1981; CLIN. PEDIATR.; ISSN 0009-9228; USA; DA. 1981; VOL. 20; NO 8; PP. 534-536; BIBL. 15 REF.Article

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter → 22ql2.1 : Clinical, cytogenetic and molecular observationsVAGLIO, Alicia; MILUNSKY, Aubrey; HUANG, Xin-Li et al.European journal of medical genetics. 2008, Vol 51, Num 4, pp 332-342, issn 1769-7212, 11 p.Article

Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter→q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and Cat eyë phenotypical featuresGABARRON, J; GLOVER, G; JIMENEZ, A et al.Clinical genetics. 1985, Vol 28, Num 6, pp 509-515, issn 0009-9163Article

Catch 22 : Microdeletion 22q11 screening in patients with congenital heart defectsVON BEUST, G; BARTMUS, D; BARTELS, I et al.Genetic counseling. 1998, Vol 9, Num 3, pp 223-227, issn 1015-8146Conference Paper

UN CAS DE TRISOMIE 22 INCOMPLETE DUE A LA MALSEGREGATION MEIOTIQUE D'UNE TRANSLOCATION FAMILIALE 11:22PESCIA G; JOTTERAND BELLOMO M; GAIDE AC et al.1981; REV. MED. SUISSE ROMANDE; ISSN 0035-3655; CHE; DA. 1981; VOL. 101; NO 4; PP. 325-329; BIBL. 6 REF.Article

TRISOMIE PARTIELLE 11Q PAR MALSEGREGATION D'UNE TRANSLOCATION MATERNELLE T(11; 22) (P23; P11.1)PANGALOS C; COUTURIER J; BARTSOCAS C et al.1980; NOUV. PRESSE MED.; ISSN 0301-1518; FRA; DA. 1980; VOL. 9; NO 41; PP. 3065-3067; ABS. ENG; BIBL. 7 REF.Article

A PROPOS D'UNE NOUVELLE OBSERVATION DE TRISOMIE 11G SECONDAIRE A UNE TRANSLOCATION MATERNELLE T(11;22) (G23.1;G11.1)CHAUVEAU P; GRUCHY D; HEROUIN C et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 4; PP. 213-215; ABS. ENG; BIBL. 14 REF.Article

HABITUAL ABORTION AND TRANSLOCATION (22Q; 22Q): UNEXPECTED TRANSMISSION FROM A MOTHER TO HER PHENOTYPICALLY NORMAL DAUGHTERKIRKELS VGHJ; HUSTINX TWJ; SCHERES JMJC et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 456-461; BIBL. 23 REF.Article

A CASE OF PARTIAL TRISOMY 22 WITHOUT CAT-EYE STIGMATAKADOTANI T; KATANO T; YAMAOKA H et al.1978; PROC. JAP. ACAD. B; JPN; DA. 1978; VOL. 54; NO 5; PP. 217-221; BIBL. 9 REF.Article

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

A (17; 22) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-119MACINTYRE MN; HEMPEL JM; WALDEN DB et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 80-81; BIBL. 2REF.Article

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

RING CHROMOSOME 22 IN A MENTALLY RETARDED CHILD AND MOSAIC 45,XX,-15, -22,+T(15; 22) (P11; Q11)/46, XX, R(22)/46, XX KAROTYPE IN THE MOTHERFRYNS JP; VANDEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 213-216; BIBL. 5 REF.Article

A Family-and Population-Based Study of the UFD1L Gene for SchizophreniaLIN XIE; LIN YE; JUN WEI et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1076-1079, issn 1552-4841, 4 p.Article

Does chromosome 22 have anything to do with sex determination: Further studies on a 46, XX, 22q11.2 del maleERICKSON, Robert P; SKINNER, Steve; JACQUET, Hélène et al.American journal of medical genetics. 2003, Vol 123A, Num 1, pp 64-67, issn 0148-7299, 4 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

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

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

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

TWO SUCCESSIVE PARTIAL TRISOMIES FOR OPPOSITE HALVES OF CHROMOSOME 22 IN A MOTHER WITH A BALANCED TRANSLOCATIONBENDEL RP; BALDINGER S; MILLARD C et al.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 313; BIBL. 2 REF.Article

DUPLICATION OF THE SEGMENT Q122->QTER OF CHROMOSOME 22 DUE TO PATERNAL INVERSION 22 (P13Q122)FUJIMOTO A; WILSON MG; TOWNER JW et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 82-84; BIBL. 3 REF.Article

THE ASSOCIATION OF THE DIGEORGE ANOMALAD WITH PARTIAL MONOSOMY OF CHROMOSOME 22KELLEY RI; ZACKAI EH; EMANUEL BS et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 101; NO 2; PP. 197-200; BIBL. 22 REF.Article

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