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kw.\*:("Supernumerary X chromosome")

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Results 1 to 25 of 668

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Triple-X syndrome and premature ovarian failureVILLANUEVA, A. L; REBAR, R. W.Obstetrics and gynecology (New York. 1953). 1983, Vol 62, Num 3, pp 70S-73S, issn 0029-7844Article

The 49,XXXXY syndrome. Clinical and psychological follow-up dataBORGHGRAEF, M; FRYNS, J. P; SMEETS, E et al.Clinical genetics. 1988, Vol 33, Num 6, pp 429-434, issn 0009-9163Article

Twenty-six years later: a woman with tetra-X chromosomesBERG, J. M; KARLINSKY, H; KOROSSY, M et al.Journal of mental deficiency research. 1988, Vol 32, pp 67-74, issn 0022-264X, 1Article

Jeunes enfants 48 XXYY. Difficultés d'établissement du diagnostic = Young children 48 XXYY. Difficult diagnosisGENEIX, A; PERISSEL, B; TURCHINI, M. F et al.Bordeaux médical. 1985, Vol 18, Num 9, pp 305-306, issn 0021-7867Article

LE SYNDROME 49, XXXXX: A PROPOS D'UN NOUVEAU CAS.TUMBA A; FRYNS JP; VAN OOTEGHEM G et al.1977; UN. MED. CANADA; CANADA; DA. 1977; VOL. 106; NO 2; PP. 226-230; ABS. ANGL.; BIBL. 8 REF.Article

Diagnosis and treatment of a child with X-polysomyRUSTAGI, P. K; FINE, P. M.Journal of the American Academy of Child Psychiatry. 1987, Vol 26, Num 4, pp 593-594, issn 0002-7138Article

A case of heredo-ataxia in a subject with karyotype 49 XXXXYSTANZANI, P; BRUNO, L; POLLARI MAGLIETTA, E et al.Brain & development (Tokyo. 1979). 1986, Vol 8, Num 5, pp 570-571, issn 0387-7604Article

A possible explanation for the low incidence of gonosomal aneuploidy among the Offspring of triplo-X individualsNERI, G.American journal of medical genetics. 1984, Vol 18, Num 2, pp 357-364, issn 0148-7299Article

LYMPHOCYTE PROLIFERATION IN A 31-WEEK PREMATURE NEONATE WITH 69, XXX CHROMOSOMAL CONSTITUTIONPITTARD WB III; SORENSEN RU; STALLARD R et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 24; NO 1; PP. 26-28; BIBL. 5 REF.Article

KARYOLOGICAL AND ANTHROPOLOGICAL ANALYSIS OF A CASE OF 47, XXX (SUPER FEMALE)HADYNA A; WOJCIECHOWSKA H.1980; FOLIA BIOL. (WARSZ.); ISSN 0015-5497; POL; DA. 1980; VOL. 28; NO 3; PP. 305-312; H.T. 1; ABS. POL/RUS; BIBL. 14 REF.Article

LETTER TO THE EDITOR: 49, XXXXY SYNDROMEPALLISTER PD.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 337-339Article

EIN NEUER FALL VON PENTASOMIE X = UN NOUVEAU CAS DE PENTASOMIE XSCHROETER C; JAHRIG K; WEINKE I et al.1980; HELV. PAEDIATR. ACTA; CHE; DA. 1980; VOL. 35; NO 3; PP. 233-241; ABS. FRE/ENG; BIBL. 25 REF.Article

WOMEN WITH TETRA-X (48, XXXX).NIELSEN J; HOMMA A; CHRISTIANSEN F et al.1977; HEREDITAS; SUEDE; DA. 1977; VOL. 85; NO 2; PP. 151-155; BIBL. 27 REF.Article

49,XXXXX SYNDROMEFRAGOSO R; HERNANDEZ A; PLASCENCIA ML et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 145-148; ABS. FRE; BIBL. 18 REF.Article

POLYSOMY X MASQUERADING AS DOWN'S SYNDROME. THE NECESSITY OF BEING EARNEST ABOUT KARYOTYPE ANALYSIS IN THE DIAGNOSIS OF MONGOLISMGARDNER LJ.1979; AMER. J. DIS. CHILD.; USA; DA. 1979; VOL. 133; NO 3; PP. 253-254; BIBL. 11 REF.Article

CHROMOSOME ANEUPLOIDY WITH XXX SYNDROME X0 TURNER'S SYNDROME AND THEIR DERMATOGLYPHIC PATTERNS.DASGUPTA J; DASGUPTA D; BISHT DB et al.1976; NUCLEUS; INDIA; DA. 1976; VOL. 19; NO 1; PP. 51-57; BIBL. 22 REF.Article

THE PENTA-X SYNDROMEMONHEIT A; FRANCKE U; SAUNDERS B et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 392-396; BIBL. 16 REF.Article

NON-DISJUNCTION OF AN UNUSUAL X CHROMOSOME.HAYATA I; OSHIMURA M; MARINELLO MJ et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 4; PP. 320-323; BIBL. 7 REF.Article

LETTER TO THE EDITOR: OBSERVATIONS ON THE NATURAL HISTORY OF 49,XXXXY INDIVIDUALSHECHT F.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 335-336Article

ECHTER XX/XY HERMAPHRODIT MIT POSITIVEN H-Y ANTIGEN OHNE AUFGEFUNDENES TESTISGEWEBE. BEOBACHTUNG VON GEBURT BIS ZUM 10-LEBENSJAHR = AUTHENTIQUE XX/XY HERMAPHRODISME, AVEC ANTIGENE H-Y POSITIF, SANS TISSU TESTICULAIRE DETECTABLE. OBSERVATION DE LA NAISSANCE A L'AGE DE 10 ANSESSER KJ; FRANK M; HILD F et al.1981; KLIN. PEDIATR.; ISSN 0300-8630; DEU; DA. 1981; VOL. 193; NO 1; PP. 13-16; ABS. ENG; BIBL. 14 REF.Article

PENTASOMIE X. A PROPOS D'UN CAS DE DECOUVERTE NEO-NATALEGOUYON JEAN BERNARD.1979; ; FRA; DA. 1979; 102; 148 P.-1 PL.: ILL.; 30 CM; H.T. 1; BIBL. 79 REF.; TH.: MED./DIJON/1979Thesis

SYNDROME DE KLINEFELTER ET PSYCHIATRIE.FRACHON BERTRAND.sd; FRA; DA. S.D.; 129; 97 P.; 30 CM; BIBL. 13 P.; TH.: MED./PARIS 5/1978Thesis

What causes the abnormal phenotype in a 49,XXXXY male?SARTO, G. E; OTTO, P. G; KUHN, E. M et al.Human genetics. 1987, Vol 76, Num 1, pp 1-4, issn 0340-6717Article

Congenital knee dislocation in a 49,XXXXY boySIJMONS, R. H; VAN ESSEN, A. J; VISSER, J. D et al.Journal of medical genetics. 1995, Vol 32, Num 4, pp 309-311, issn 0022-2593Article

Two 48,XXYY patients: clinical, cytogenetic and molecular aspectsZELANTE, L; PIEMONTESE, M. R; FRANCIOLI, G et al.Annales de génétique (Paris). 2003, Vol 46, Num 4, pp 479-481, issn 0003-3995, 3 p.Article

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