Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("ABNORMAL G21 CHROMOSOME")

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 551

  • Page / 23

Export

Selection :

  • and

A case of 21q: syndrome with half normal SOD-1 activityYOSHIMITSU, K; HATANO, S; KOBAYASHI, Y et al.Human genetics. 1983, Vol 64, Num 2, pp 200-202, issn 0340-6717Article

INTERSTITIAL DELECTION OF CHROMOSOME 21MODI N; BUCKTON KE.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 4; PP. 215-219; BIBL. 28 REF.Article

A CASE OF R(21) WITH STIGMATA OF ATYPICAL DOWN SYNDROMEIESHIMA A; OGA SAWARA N; YAMAMOTO Y et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 65-69; BIBL. 18 REF.Article

Q-: A CANDIDATE CHROMOSOME MARKER OF PRIMARY THROMBOCYTHEMIAZACCARIA A; BACCARANI M; GUGLIOTTA L et al.1978; HAEMATOLOGICA; ITA; DA. 1978; VOL. 63; NO 3; PP. 337-338; BIBL. 6 REF.Article

CONTRIBUTION A L'ETUDE DE LA TRISOMIE 21 PARTIELLE. A PROPOS DE 3 CAS.GERBAUD CENNI D.1978; MARSEILLE; ASSOC. ANCIENS EXTERNES HOP.; DA. 1978; PP. 1-53; H.T. 15; BIBL. 5 P. 1/2; (THESE DOCT. MED.; PARIS V)Thesis

THREE INTERESTING CASES OF DOWN SYNDROMEPEREZ CASTILLO A; DEL MAZO J; ABRISQUETA JA et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 123-128; ABS. FRE; BIBL. 24 REF.Article

21Q-IN PRIMARY THROMBOCYTHEMIAZACCARIA A; BACCARANI M; GUGLIOTTA L et al.1980; CANCER GENET. CYTOGENET.; USA; DA. 1980; VOL. 1; NO 4; PP. 337-344; BIBL. 33 REF.Article

I/21 TRANSLOCATION.MILLER JQ; WILLSON K; GOLDBERG MJ et al.1977; SOUTH. MED. J.; U.S.A.; DA. 1977; VOL. 70; NO 1; PP. 102-104; BIBL. 6 REF.Article

MONOSOMIA PARZIALE DI UN CROMOSOMA DEL GRUPPO G (21 Q-) ASSOCIATA A NANISMO MESOMELICO A TRASMISSIONE AUTOSOMICA DOMINANTE. = MONOSOMIE PARTIELLE D'UN CHROMOSOME DU GROUPE G (21 Q-)-ASSOCIEE A UN MANISME MESOMELIQUE A TRANSMISSION AUTOSOMIQUE DOMINANTEDUILLO MT.1977; MINERVA PEDIATR.; ITAL.; DA. 1977; VOL. 29; NO 21; PP. 1341-1348; ABS. ANGL.; BIBL. 1 P.Article

MATERNALLY TRANSMITTED EXTRA RING (21) CHROMOSOME IN A BOY WITH DOWN'S SYNDROMEMATSUBARA T; NAKAGOME Y; OGASAWARA N et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 78-79; BIBL. 12 REF.Article

ZUR AETIOLOGIE DES MONGOLISMUS = L'ETIOLOGIE DU MONGOLISMEWAGENBICHLER P.1981; NATURWISSENSCHAFTEN; ISSN 0028-1042; DEU; DA. 1981; VOL. 68; NO 2; PP. 76-81; ABS. ENG; BIBL. 40 REF.Article

TRISOMIE 21 PAR DUPLICATION EN MIROIR 46, XX, PSU DIC(21) TER REA (21 Q 21 Q)TURLEAU C; ROUBIN M; CHAVIN COLIN F et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 187-189; ABS. ENG; BIBL. 19 REF.Article

A CHROMOSOMAL ABNORMALITY (219) IN PRIMARY THROMBOCYTOSISPETIT P; VANDEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 105-106; BIBL. 1 REF.Article

A CASE OF ATYPICAL DOWN'S SYNDROME WITH MOSAIC 46, XX/46, XX-21+T(21Q21Q).HORNSTEIN L; SOUKUP S.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 77-81; BIBL. 22 REF.Article

RING CHROMOSOME 21 SYNDROME: A MALFORMED NEWBORN INFANT WITH 45, XY, -21/46, XY, 21R MOSAICISMFRYNS JP; PETIT P; DE BACKER S et al.1981; ACTA PAEDIATRICA BELGICA; ISSN 0001-6535; BEL; DA. 1981; VOL. 34; PP. 245-247; BIBL. 8 REF.Article

T(21Q21Q)/R(T(21Q21P)) MOSAIC IN TWO UNRELATED PATIENTS WITH MILD STIGMATA OF DOWN'S SYNDROMEDALLAPICCOLA B; BIANCO I; BRINCHI V et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 56-58; ABS. ENG; BIBL. 4 REF.Article

A CASE OF DOWN'S SYNDROME RESULTING FROM MIRROR DUPLICATION OF CHROMOSOME 21STOLL C; PENNERATH A; LAUSECKER C et al.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 1; PP. 80-81; BIBL. 12 REF.Article

DESCRIZIONE DI UN CASO DI TRISOMIA 21 CON TRASLOCAZIONE = DESCRIPTION D'UN CAS DE TRISOMIE 21 PAR TRANSLOCATIONGRIMOLDI MG; LAVEZZI AM.1981; FOLIA HERED. PATHOL.; ISSN 0015-5578; ITA; DA. 1981; VOL. 30; NO 2; PP. 21-25; ABS. ENG; BIBL. 5 REF.Article

STRUCTURAL CHROMOSOME ABNORMALITIES IN DOWN SYNDROME: A STUDY OF TWO FAMILIES.JOCOBS PA; MAYER M; RUDAK E et al.1978; CYTOGENET. CELL GENET.; SWITZ.; DA. 1978; VOL. 20; NO 1-6; PP. 185-193; BIBL. 15 REF.Article

TWO CASES OF DOWN SYNDROME WITH UNUSUAL DE NOVO TRANSLOCATION.VERMA RS; PEAKMAN DC; ROBINSON A et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 227-234; BIBL. 12 REF.Article

ANALYSIS OF BANDING PATTERNS IN A CASE OF RING CHROMOSOME 21RICHER CL; FITCH N; SITAHAL S et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 4; PP. 323-331; BIBL. 45 REF.Article

DOWN SYNDROME DUE TO PARTIAL TRISOMY 21Q.CERVENKA J; GORLIN RJ; DJAVADI GR et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 2; PP. 119-121; BIBL. 9 REF.Article

Ring chromosome 21 in a normal femaleKLECZKOWSKA, A; FRYNS, J. P.Annales de génétique (Paris). 1984, Vol 27, Num 2, pp 126-128, issn 0003-3995Article

Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemiaWERNER-FAVRE, C; CABROL, C; BERIS, P et al.Annales de génétique (Paris). 1983, Vol 26, Num 4, pp 240-242, issn 0003-3995Article

Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and ItalySCHMID, W; TENCONI, R; BACCICHETTI, C et al.American journal of medical genetics. 1983, Vol 16, Num 3, pp 323-329, issn 0148-7299Article

  • Page / 23