DELETION FROM THE LONG ARM OF CHROMOSOME 4 (46, XX, 4Q-) ASSOCIATED WITH CONGENITAL ANOMALIES = DELETION DU BRAS LONG DU CHROMOSOME 4 (46, XX, 4Q-) ASSOCIEE A DES ANOMALIES CONGENITALESGOLBUS MS; CONTE FA; DAENTL DL et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 1; PP. 83-85; BIBL. 10 REF.Serial Issue

LE SYNDROME 18Q. ETUDE D'UN CAS DE DELETION PARTIELLE DU BRAS LONG CHROMOSOME 18CASTEL Y; RIVIERE D; DARIDON F et al.1973; REV. INTERNATION. PEDIATR.; FR.; DA. 1973; NO 33; PP. 21-40(13P.); BIBL. 2P.Serial Issue

NORMAL MALE DEVELOPMENT WITH Y CHROMOSOME LONG ARM DELETION (YQ-) = DEVELOPPEMENT MALE NORMAL EN PRESENCE D'UNE DELETION DU BRAS LONG DU CHROMOSOME Y (YQ-)MEISNER LF; INHORN SL.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 373-377; BIBL. 12 REF.Serial Issue

A PHENOTYPIC MALE WITH KARYOTYPE 45,X/45,X,ACE+ (.YQ-) = UN MALE PHENOTYPIQUE DE CARYOTYPE 45,X/45,X,ACE+ (.YQ-)NIELSEN J; FRIEDRICH U; CHRISTENSEN AL et al.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 15; NO 4; PP. 319-326; ABS. ALLEM.; BIBL. 9REF.Serial Issue

OCCURRENCE OF MENTAL RETARDATION IN PATIENTS WITH RETINOBLASTOMA = SURVENUE DE RETARD MENTAL CHEZ DES MALADES AYANT UNE RETINOBLASTOMETARKKANEN A.1973; ACTA OPHTHALMOL.; DANEM.; DA. 1973; VOL. 51; NO 1; PP. 67-71; BIBL. 11REF.Serial Issue

THE SYNDROME ASSOCIATED WITH THE PARTIAL DELETION OF THE LONG ARMS OF CHROMOSOME 18 (18Q-) = SYNDROME ASSOCIE A LA DELETION PARTIELLE DU BRAS LONG DU CHROMOSOME 18 (18Q-)PARKER CE; JAMSHED MAVALWALA; KOCH R et al.1972; CALIFORNIA MED.; U.S.A.; DA. 1972; VOL. 117; NO 4; PP. 65-71; BIBL. 26 REF.Serial Issue

RING-CHROMOSOM 18. EIN 18P-/18Q-DELETIONSSYNDROM = CHROMOSOME 18 EN ANNEAU. UN SYNDROME DE DELETION 18P-/18Q-KUNZE J; STEPHAN E; TOLKSDORF M et al.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 15; NO 4; PP. 289-318; ABS. ANGL.; BIBL. 6P.Serial Issue

LA MENOPAUSA PRECOCE: ULTERIORE CONTRIBUTO CASISTICO E PRESENTAZIONE DI DUE CASI CON ANOMALIE CROMOSOMICHE (XX/XO E XXQ-) = MENOPAUSE PRECOCE: NOUVELLE CONTRIBUTION A L'ETUDE DES CAS ET PRESENTATION DE 2 CAS AVEC ANOMALIE CHROMOSOMIQUE XX/XO ET XXQ-MONETA E; GARCIA N; CAPPA F et al.1972; FOLIA ENDOCRINOL.; ITAL.; DA. 1972; VOL. 25; NO 5; PP. 364-381; ABS. FR. ANGL.; BIBL. 24 REF.Article

PATHOLOGICAL CHANGES IN CONGENITAL DEAFNESS = MODIFICATIONS ANATOMOPATHOLOGIQUES DANS LA SURDITE CONGENITALEBERGSTROM L; HEMENWAY WG; SANDO I et al.1972; LARYNGOSCOPE; U.S.A.; DA. 1972; VOL. 82; NO 10; PP. 1777-1792; BIBL. 13REF.Serial Issue

LONG-ARM DELETION OF CHROMOSOME 22, WITH PROTEINLESING ENTEROPATHY = DELETION DES BRAS LONGS DU CHROMOSOME 22 AVEC PROTIDORRHEE INTESTINALENELSON R.1972; PROC. R. SOC. MED.; G.B.; DA. 1972; VOL. 65; NO 12; PP. 1081-1083; BIBL. 2REF.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