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kw.\*:("Chromosome X surnuméraire")

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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

A CASE REPORT ON X-TRISOMY IN CATTLENORBERG HS; REFSDAL AO; GARM ON et al.1976; HEREDITAS; SUEDE; DA. 1976; VOL. 82; NO 1; PP. 69-72; BIBL. 8 REF.Article

GENE DOSAGE COMPENSATION IN METAFEMALES (3X; 2A) OF DROSOPHILALUCCHESI JC; RAWLS JM JR; MARONI G et al.1974; NATURE; G.B.; DA. 1974; VOL. 248; NO 5449; PP. 564-567; BIBL. 20REF.Article

XXYY SON OF A TRIPLE-X MOTHER = LE FILS XXYY D'UNE MERE TRIPLO-XZIZKA J; BALICEK P; NIELSEN J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 2; PP. 159-160; BIBL. 4REF.Article

MOSAICO 45, X/46, XX47, XXX. = MOSAIQUE 45, X/46, XX/47, XXXANSEDE A; COUSELO JM; ALVEZ F et al.1975; REV. ESP. PEDIATR.; ESP.; DA. 1975; VOL. 31; NO 185; PP. 685-692; ABS. FR. ANGL. ALLEM.; BIBL. 12 REF.Article

SEX CHROMOSOME ANEUPLOIDY AMONG MEN IN THREE SWEDISH HOSPITAL FOR THE MENTALLY RETARDED AND MALADJUSTED = ANEUPLOIDIE DES CHROMOSOMES SEXUELS CHEZ DES SUJETS DE SEXE MASCULIN DE 3HOPITAUX SUEDOIS POUR LES RETARDES MENTAUX ET LES INADAPTESAKESSON HO; FORSSMAN H; WAHLSTROEM J et al.1974; BRIT. J. PSYCHIATRY; G.B.; DA. 1974; VOL. 125; PP. 386-389; BIBL. 9REF.Article

EXAMEN BIOMETRIQUE DES SUJETS XXXXY, DE LEURS PARENTS ET DE LEURS GERMAINSTUMBA A.1974; UN. MED. CANADA; CANADA; DA. 1974; VOL. 103; NO 10; PP. 1729-1735; ABS. ANGL.; BIBL. 3REF.Article

PREMATURE CENTROMERE DIVISION: A MECHANISM OF NON-DISJUNCTION CAUSING X CHROMOSOME ANEUPLOIDY IN SOMATIC CELLS OF MAN = LA DIVISION PREMATUREE DU CENTROMERE, UN MECANISME DE NON-DISJONCTION CAUSE D'ANEUPLOIDIE DU CHROMOSOME X DANS LES CELLULES SOMATIQUES HUMAINESFITZGERALD FH; PICKERING AF; MERCER JM et al.1975; ANN. HUM. GENET.; G.B.; DA. 1975; VOL. 38; NO 4; PP. 417-428; BIBL. 7 REF.Article

49, XXXXY PATIENT WITH HEMIFACIAL MICROSOMIA. = UN MALADE 49, XXXXY AVEC UNE MICROSOMIE HEMIFACIALEKUSHNICK T; COLONDRILLO M.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 7; NO 5; PP. 442-448; BIBL. 17 REF.Article

SELF-MUTILATION IN A CASE OF 49,XXXXY CHROMOSOMAL CONSTITUTIONKORTEN JJ; VANDORP A; HUSTINX TWJ et al.1975; J. MENTAL DEFIC. RES.; G.B.; DA. 1975; VOL. 19; NO 1; PP. 63-71; BIBL. 20 REF.Article

A MECHANISM OF X CHROMOSOME ANEUPLOIDY IN LYMPHOCYTES OF AGING WOMEN = MECANISME DE L'ANEUPLOIDIE DU CHROMOSOMEX DANS LES LYMPHOCYTES DE FEMME AGEEFITZGERALD PH.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 2; PP. 153-158; BIBL. 9REF.Article

48,XXX,+18 DOUBLE TRISOMYMADAHAR DP; DOSIK H; WELLER I et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 309-311; BIBL. 10 REF.Article

STUDIES OF MALFORMATION SYNDROMES IN MAN XXX: MULTIPLE CONGENITAL ANOMALIES/MENTAL RETARDATION SYNDROME OF VARIANT FAMILIAL DEVELOPMENTAL PATTERN; DIFFERENTIAL DIAGNOSIS AND DESCRIPTION OF THE MCDONOUGH SYNDROME (WITH XXY SON FROM XY/XXY FATHER) = ETUDES SUR LES SYNDROMES MALFORMATIFS XXX CHEZ L'HOMME: SYNDROME DE MALFORMATIONS CONGENITALES, DE RETARD MENTAL DE DEVELOPPEMENT FAMILIAL VARIE; DIAGNOSTIC DIFFERENTIEL ET DESCRIPTION DU SYNDROME DE MCDONOUGH (AVEC FILS XXY DE PERE XY/XXY)NEUHAUSER G; OPITZ JM.1975; Z. KINDERHEILKDE; DTSCH.; DA. 1975; VOL. 120; NO 4; PP. 231-242; BIBL. 18 REF.Article

UNE OBSERVATION DE TRIPLE MOSAIQUE CHROMOSOMIQUE XXY/XXXY/XXXXYTUMBA A.1975; UN. MED. CANADA; CANADA; DA. 1975; VOL. 104; NO 5; PP. 739-744; ABS. ANGL.; BIBL. 6 REF.Article

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

LE SYNDROME XXXX A PROPOS D'UN NOUVEAU CAS OBSERVE DES LA NAISSANCE.TUMBA A; FRIJNS JP; TIMMERMAN J et al.1975; UN. MED. CANADA; CANADA; DA. 1975; VOL. 104; NO 8; PP. 1211-1214; ABS. ANGL.; BIBL. 21 REF.Article

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

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

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

KLINEFELTER'S SYNDROME AND MATERNAL XX/XXX MOSAICISM = SYNDROME DE KLINEFELTER ET MOSAIQUE MATERNELLE XX/XXXTSUANG MT; MILLER JR; DE BAULT LE et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 1; PP. 114; BIBL. 9REF.Article

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