DELETION OF THE SHORT ARM OF CHROMOSOME #9 (46, 9P-): A NEW DELETION SYNDROMEALFI O; DONNELL GN; CRANDALL BF et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 17-22; ABS. FR.; BIBL. 19REF.Serial Issue

A CASE OF THE 18P-SYNDROMESUBRT I; BERANKOVA J.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 16; NO 4; PP. 359-360Serial Issue

18P-SYNDROMET. DELETION AF DEN KORTE ARM AF KROMOSOM NR. 18 = SYNDROME 18P-. DELETION DU BRAS COURT DU CHROMOSOME 181973; UGESKR. LAEGER; DANM.; DA. 1973; VOL. 135; NO 1; PP. 17; BIBL. 5REF.Serial Issue

PARTIELLE DELETION DES KURZEN ARMES EINES CHROMOSOMES 4 (WOLF-SYNDROM). ZWEI NEUE FAELLE = DELETION PARTIELLE DU BRAS COURT D'UN CHROMOSOME 4 (SYNDROME DE WOLF). DEUX NOUVEAUX CASSCHINZEL A; SCHMID W.1972; ARCH. GENET.; SCHWEIZ; DA. 1972; VOL. 45; NO 2; PP. 88-98; ABS. ANGL.; BIBL. 19REF.Serial Issue

MALFORMAZIONI SCHELETRICHE DA ABERRAZIONI CROMOSOMICHE = LES MALFORMATIONS SQUELETTIQUES DANS LES ABERRATIONS CHROMOSOMIQUESDALLAPICCOLA B; PISTOCCHI GF.1972; MINERVA MED.; ITAL.; DA. 1972; VOL. 63; NO 92; PP. 5049-5268; ABS. ANGL.; BIBL. 15REF.Serial Issue