Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("CHROMOSOME X ANORMAL")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 969

  • Page / 39
Export

Selection :

  • and

DIFFERENCES IN HUMAN X ISOCHROMOSOMESPRIEST JH; BLACKSTON RD; AU KS et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 378-389; BIBL. 23 REF.Article

AN (X; 3) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-194DE LA CHAPELLE A; SCHROEDER J; KLINGER HP et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 404-405; BIBL. 1 REF.Article

DELETION MAPPING OF THE HUMAN X CHROMOSOME. = CARTE DU CHROMOSOME X HUMAIN D'APRES L'ETUDE DE DELETIONSDE LA CHAPELLE A; SCHRODER J; HAAHTELA T et al.1975; HEREDITAS; SUEDE; DA. 1975; VOL. 80; NO 1; PP. 113-120; BIBL. 22 REF.Article

FUSION OF THE SHORT ARMS OF ONE X CHROMOSOME IN A PATIENT WITH GONADAL DYSGENESIS = FUSION DES BRAS COURTS D'UN CHROMOSOME X CHEZ UNE MALADE ATTEINTE DE DYSGENESIE GONADIQUERUTHNER U; GOLOB E.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 2; PP. 159-160; BIBL. 1 REF.Article

UN DEUXIEME EXEMPLE DE FUSION TELOMERIQUE DE DEUX CHROMOSOMES XFRAISSE J; LAURENT C; COLLARD N et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 243-245; ABS. ANGL.; BIBL. 6 REF.Article

CYTOGENETIC FINDINGS IN 89 CASES OF TURNER'S SYNDROME WITH ABNORMAL KARYOTYPES = OBSERVATIONS CYTOGENETIQUES DANS 89 CAS DE SYNDROME DE TURNER AVEC CARYOTYPE ANORMALSCHMID W; NAEF E; MUERSET G et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 2; PP. 93-104; ABS. ALLEM.; BIBL. 1P.Article

REAPPRAISAL OF A 46, X, I(XP) KARYOTYPE AS 46, X, DEL(XQ).DE LA CHAPELLE A; SCHRODER J.1975; HEREDITAS; SUEDE; DA. 1975; VOL. 80; NO 1; PP. 137-140; BIBL. 11 REF.Article

GENETIC INSTABILITY IN DROSOPHILA MELANOGASTER. EVIDENCE FOR INSERTION MUTATIONSRASMUSON B; GREEN MM; KARLSSON BM et al.1974; MOLEC. GEN. GENET.; GERM.; DA. 1974; VOL. 133; NO 3; PP. 237-247; BIBL. 15REF.Article

CONTRIBUTION A L'ETUDE DE L'INACTIVATION D'UN CHROMOSOME X CHEZ LA FEMMEGILGENKRANTZ S; ALEXANDRE P; SABORIO M et al.1974; C.R. SOC. BIOL.; FR.; DA. 1974; VOL. 168; NO 8-9; PP. 1063-1067; ABS. ANGL.; BIBL. 18 REF.Article

AN (X; 1) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-97PUNNETT HH; KISTERMACHER ML; GREENE AE et al.1974; CYTOGENET. CELL GENET; SWITZ.; DA. 1974; VOL. 13; NO 4; PP. 406-407; BIBL. 1 REF.Article

NOTES ON CLINICAL FEATURES OF A 46, XXP-PATIENTISHITOBI K; NAKADA N; WATANABE A et al.1982; PROCEEDINGS OF THE JAPAN ACADEMY. SERIES B: PHYSICAL AND BIOLOGICAL SCIENCES; ISSN 0386-2208; JPN; DA. 1982; VOL. 63; NO 2; PP. 25-28; BIBL. 10 REF.Article

STRUCTURAL ABNORMALITIES OF THE X-CHROMOSOME IN A HEIFERGENEST P; GUAY P.1979; REV. CANAD. MED. COMP.; CAN; DA. 1979; VOL. 43; NO 1; PP. 110-111; ABS. FRE; BIBL. 3 REF.Article

CLINICAL CONSEQUENCES OF XP-EGOZCUE J.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 141-142; BIBL. 15 REF.Article

X LONG ARM DELETION WITH OLIGOMENORRHOEAMIJIN K; STOLEVIC E; ADZIC S et al.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 305-306; BIBL. 13 REF.Article

FUSION OF TWO APPARENTLY INTACT HUMAN X CHROMOSOMESSINHA AK; PATHAK S; NORA JJ et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 3; PP. 295-300; BIBL. 17 REF.Article

MARKER X SYNDROMEHOWARD PEEBLES PN.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 407-408; BIBL. 6 REF.Article

CYTOGENETIC INVESTIGATION OF SIX PATIENTS WITH X ISOCHROMOSOMES, I(XQ), AND OF TWO SUBJECTS WITH ISODICENTRIC X CHROMOSOMES, IDIC(XQ)GAAL M; LASZLO J; BOESZE P et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 362-365; BIBL. 22 REF.Article

HETEROMORPHIC X CHROMOSOMES IN 46, XX MALES.DE LA CHAPELLE A; SIMOLA K; SIMOLA P et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 157-167; BIBL. 10 REF.Article

STRUCTURAL X-CHROMOSOME ABNORMALITY IN A FEMALE WITH GONADAL DYSGENESIS = ANOMALIE DE STRUCTURE DU CHROMOSOME X CHEZ UNE FEMME ATTEINTE DE DYSGENESIE GONADIQUEKRISTENSEN H; FRIEDRICH U; LARSEN G et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 2; PP. 133-138; ABS. ALLEM.; BIBL. 15REF.Article

CHROMOSOME X ET REPLICATION TARDIVE. ESSAI D'INTERPRETATION A L'AIDE DE CAS PATHOLOGIQUES ET DES TECHNIQUES CYTOGENETIQUES AVEC AUTORADIOGRAPHIE ET B.U.D.R.GILGENKRANTZ S; ALEXANDRE P; BAUE G et al.1975; LYON MED.; FR.; DA. 1975; VOL. 233; NO 3; PP. 231-240; ABS. ANGL.; BIBL. 1P.1/2Article

INCREASED Q FLUORESCENCE OF AN INACTIVE XQ-CHROMOSOME IN MAN = FLUORESCENCE Q PLUS INTENSE D'UN CHROMOSOME HUMAIN XQ-INACTIFSARTO GE; THERMAN E; PATAU K et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 4; PP. 289-293; BIBL. 12REF.Article

THE TURNER PHENOTYPE AND THE DIFFERENT TYPES OF HUMAN X ISOCHROMOSOMEOTTO PG; VIANNA MORGANTE AM; OTTO PA et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 159-164; BIBL. 32 REF.Article

46, X, DEL(X) (P21) IN A 14-YEAR-OLD FEMALE WITH TURNER SIGNS, ONE STREAK AND ONE NORMAL OVARYCRISALLI M; CUOCO C; GIMELLI G et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 2; PP. 114-116; ABS. FRE; BIBL. 10 REF.Article

INACTIVATION OF ONE OF THE X CHROMOSOMES IN FEMALES IS A BIOLOGICAL PHENOMENON OF CLINICAL IMPORTANCEBERG K.1979; ACTA MED. SCAND; SWE; DA. 1979; VOL. 206; NO 1-2; PP. 1-3; BIBL. 7 REF.Article

RELATION ENTRE ISOCHROMOSOME XQ ET DEFICIT SERIQUE EN IMMUNOGLOBULINE ACHOUDAT D; TAILLEMITE JL; HIRSCH MARIE H et al.1979; NOUV. PRESSE MED.; FRA; DA. 1979; VOL. 8; NO 29; PP. 2419; BIBL. 4 REF.Article

  • Page / 39