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A (2;4) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-1064.BIEDERMAN B; BOWEN P; ARONSON MM et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 5; PP. 300-301; BIBL. 1 REF.Article

UNEINHEITLICHER PHAENOTYP BEI PARTIALTRISOMIE 4Q = VARIATION PHENOTYPIQUE DANS LA TRISOMIE 4Q PARTIELLEVOGEL W; SIEBERS JW; GUNKEL J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 2; PP. 103-112; ABS. ALLEM.; BIBL. 19REF.Article

TRANSLOCATION OF CHROMOSOME 4 AND 9 WITH RING FORMATION OF CHROMOSOME 4 SHORT ARMBERNSTEIN R; MILNE AT; JENKINS T et al.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 4; PP. 310-314; BIBL. 16 REF.Article

PARTIAL TRISOMY 4Q DUE TO FAMILIAL 2/4 TRANSLOCATION.BIEDERMAN B; BOWEN P.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 147-153; BIBL. 16 REF.Article

REPLICATION PATTERN OF THE X CHROMOSOMES IN THREE X/AUTOSOMAL TRANSLOCATIONS.HAGEMEIJER A; HOOVERS J; SMIT EME et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 6; PP. 333-348; BIBL. 2 P.Article

TRISOMY 4G32->4GTER DUE TO A MATERNAL 4/21 TRANSLOCATIONBACCICHETTI C; TENCONI R; ANGLANI F et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 425-427; BIBL. 9 REF.Article

TRISOMIA 4P DA TRASLOCAZIONE T (4 P-, 22P+). INDAGINE FAMILIARE SU QUATTRO GENERAZIONI = TRISOMIE 4P PAR TRANSLOCATION T (4P-, 22P+). ETUDE FAMILIALE SUR 4 GENERATIONSFORABOSCO A; GIOVANNELI G; MARZONA L et al.1976; MINERVA PEDIATR.; ITAL.; DA. 1976; VOL. 28; NO 12; PP. 743-751; ABS. ANGL.; BIBL. 6 REF.Article

TRISOMY 4P IN A FAMILY WITH A T (4;15)HUSTINX TWJ; GABREELS FJM; KIRKELS VGHJ et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 13-19; ABS. FR.; BIBL. 25REF.Article

LA TRISOMIE 4Q PARTIELLE. A PROPOS DE TROIS OBSERVATIONSDUTRILLAUX B; LAURENT C; FORABOSCO A et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 21-27; ABS. ANGL.; BIBL. 7REF.Article

Interstitial deletion of the long arm of chromosome 4CHUDLEY, A. E; VERMA, M. R; RAY, M et al.American journal of medical genetics. 1988, Vol 31, Num 3, pp 549-551, issn 0148-7299Article

Un diagnostic cytogénétique difficile de monosomie 4p = A difficult prenatal diagnosis of 4p monosomyVITTU, G; CROQUETTE, M. F; BOIDEIN, F et al.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 75-82, issn 0021-7743Conference Paper

THE WOLF-HIRSCHHORN (4P-) SYNDROME.JOHNSON VP; MULDER RD; HOSEN R et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 104-112; BIBL. 2 P.Article

A third case of de novo partial trisomy 4 pOORTHUYS, J. W. E; GERSSEN-SCHOORL, K. B. J; DE PATER, J. M et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 344-345, issn 0022-2593, 2 p.Article

SINDROMES 4P-Y 5P-(SU IDENTIFICACION POR EL ESTUDIO CROMOSOMICO). = SYNDROMES 4P- ET 5P. LEUR IDENTIFICATION PAR L'ETUDE CHROMOSOMIQUEPRIETO F; BADIA L; ORELLANA F et al.1975; REV. ESP. PEDIATR.; ESP.; DA. 1975; VOL. 31; NO 184; PP. 581-590; ABS. FR. ANGL. ALLEM.; BIBL. 1 P.Article

A (4;21) TRANSLOCATION, UNBALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-98SEABRIGHT M; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 152-153Article

A NEW CHROMOSOME ANOMALY IN ACUTE LYMPHOBLASTIC LEUKEMIA (ALL)VAN DEN BERGHE H; DAVID G; BROECKAERT VAN ORSHOVEN A et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 2; PP. 173-180; BIBL. 1 P.Article

NEW AUTOSOMAL SYNDROMES: TRISOMIES 4 P AND 9 P.DALLAPICCOLA B; MASTROIACOVO P; SEGNI G et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 267-273; ABS. ITAL. FR. ALLEM.; BIBL. 9 REF.Article

A (4; 7) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-1220.JACKSON LG; BOZARTH B; ARONSON MM et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 19; NO 1; PP. 50Article

A TRISOMY FOR 10924-QTER FROM A FAMILIAL TRANSLOCATION: T(4;10) (Q33;Q24) IN BOTH GRANDPARENTS.OSZTOVICS M; KASZAS T.1977; ACTA PAEDIATR. ACAD. SCI. HUNGAR.; HONGR.; DA. 1977; VOL. 18; NO 3-4; PP. 201-206; ABS. RUSSE; BIBL. 15 REF.Article

A FAMILIAL TRANSLOCATION 411: T(4;11) (Q22;Q24) IDENTIFIED BY MEANS OF G-BANDS.ARCHIDIACONO N; DE CAPOA A; FERRARO M et al.1975; ATTI ACCAD. NAZION. LINCEI, R.C., CL. SCI. FIS. MAT. NAT.; ITAL.; DA. 1975 PARU 1976; VOL. 59; NO 1-2; PP. 141-146; ABS. ITAL.; BIBL. 12 REF.Article

CONSTITUTIONAL CHROMOSOMAL ABERRATION, T(4;12) (Q23;P11), IN A PATIENT WITH PH¹ POSITIVE CHRONIC MYELOCYTIC LEUKEMIAGAHRTON G; FRIBERG K; ZECH L et al.1978; HEREDITAS; SWE; DA. 1978; VOL. 89; NO 2; PP. 169-173; BIBL. 19 REF.Article

MAJOR KARYOTYPIC ABNORMALITY IN A CHILD BORN TO A WOMAN WITH UNTREATED MALIGNANT MELANOMA.FITZGERALD PH; MIETHKE P; CASELEY RT et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 3; PP. 155-161; BIBL. 3 REF.Article

4 Q-SYNDROMETOWNES PL; WHITE M; DI MARZO S et al.1979; AMER. J. DIS. CHILD.; USA; DA. 1979; VOL. 133; NO 4; PP. 383-385; BIBL. 6 REF.Article

A 3/4 RECIPROCAL TRANSLOCATION IN TWO UNRELATED FAMILIES.TENCHINI ML; MONTALI E; SIMONI G et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 2; PP. 235-238; BIBL. 5 REF.Article