A 1Q42 DELETION IN A VIETNAMESE INFANTNEU RL; AVILA DA; REDDINGTON JM et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 154-155; ABS. FRE; BIBL. 2 REF.Article

SEGREGATION OF A T(14Q22Q) CHROMOSOME IN A LARGE KINDRED = SEGREGATION D'UN CHROMOSOME T(14Q22Q) DANS UNE GRANDE FAMILLENEU RL; VALENTINE FA; GARDNER LI et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 1; PP. 30-36; BIBL. 14 REF.Article

CHROMOSOME ANALYSIS IN CASES WITH REPEATED SPONTANEOUS ABORTIONSNEU RL; ENTES K; BANNERMAN RM et al.1979; OBSTETR. AND GYNECOL.; USA; DA. 1979; VOL. 53; NO 3; PP. 373-375; BIBL. 6 REF.Article

A CASE OF CYCLOPIA WITH D TRISOMY.NEU RL; GRANT JF; GARDNER LI et al.1977; AMER. J. OBSTETR. GYNECOL.; U.S.A.; DA. 1977; VOL. 127; NO 2; PP. 212-213; BIBL. 2 REF.Article

AT (5P-;21Q+) TRANSLOCATION IN A FAMILY WITH DOWN SYNDROME.NEU RL; DEGEORGE FV; GARDNER LI et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 2; PP. 111-113; BIBL. 1 REF.Article

LONG SURVIVAL IN TRISOMY-13-SYNDROME: 21 CASES INCLUDING PROLONGED SURVIVAL IN TWO PATIENTS 11 AND 19 YERS OLDREDHEENDRAN R; NEU RL; BANNERMAN RM et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 2; PP. 167-172; BIBL. 7 REF.Article

A CASE OF 46,XY,T(3Q-;14Q+) MAT = UN CAS DE 46,XY,T(3Q-;14Q+) MAT.NEU RL; BARLOW MJ JR; GARDNER LI et al.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 2; PP. 158-161; BIBL. 7REF.Serial Issue

AN INFANT WITH TRISOMY 9 PTER-9922 RESULTING FROM 3:1 SEGREGATION IN A 46,XX,T(1; 9) (P36; 922) MOTHERNEU RL; DENNIS NR; LANMAN JT JR et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 151-154; ABS. FRE; BIBL. 9 REF.Article

,YY/46, XY, 21Q-MOSAICISM IN AN INFANT WITH NEUTROPENIA AND PROPERDIN DEFICIENCY.NEU RL; STOCKMAN JA III; SPITER RE et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 4; PP. 332-334; BIBL. 8 REF.Article

THREE GENERATIONS AND SIX FAMILY MEMBERS WITH AT(13Q15Q) CHROMOSOME = TROIS GENERATIONS ET SIX MEMBRES D'UNE FAMILLE AVEC UN CHROMOSOME T(13Q15Q)NEU RL; GARDNER LI; WILLIAMS ML et al.1973; J. MED. GENET; G.B.; DA. 1973; VOL. 10; NO 1; PP. 94-96; BIBL. 4 REF.Serial Issue

AN INFANT WITH TRISOMY 6Q21->6QTERNEU RL; GALLIEN JU; STEINBERG WARREN N et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 167-169; ABS. FRE; BIBL. 2 REF.Article

INCLUSION OF SATELLITES IN AN 18/21 TRANSLOCATION CHROMOSOME SHOWN BY AMMONIACAL-SILVER STAINING (SAT-BANDING) IN CASE OF PARTIAL TRISOMY 18.NEU RL; ORTEGA CC; BARG GA et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 520-522; BIBL. 17 REF.Article

AN INFANT WITH DUPLICATION OF 17Q21->17 QTERGALLIEN JU; NEU RL; WYNN RJ et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 1; PP. 111-115; BIBL. 2 REF.Article