CLINICAL FEATURES OF MONOSOMY 10QTERZATTERALE A; PAGANO L; FIORETTI G et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 106-108; ABS. FRE; BIBL. 17 REF.Article

TERMINAL DELECTION OF THE LONG ARM OF CHROMOSOME 10: Q26->QTER: CASE REPORT AND REVIEW OF LITERATURETAYSI K; STRAUSS AW; YANG V et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 141-144; ABS. FRE; BIBL. 3 REF.Article

RING CHROMOSOME 10: 46, XX, R (10) (P15->Q26)TSUKINO R; TSUDA N; DEZAWA T et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 2; PP. 148-151; BIBL. 4 REF.Article

A CASE OF 10P- SYNDROMESUCIU S; NANULESCU M.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 109-111; ABS. FRE; BIBL. 11 REF.Article

PHENOTYPE ASSOCIATED WITH RING 10 CHROMOSOME: REPORT OF PATIENT AND REVIEW OF LITERATUREMICHELS VV; DRISCOLL DJ; LEDBETTER DH et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 231-237; BIBL. 11 REF.Article

DUPLICATION DEFICIENCY AS THE RESULT OF MEIOTIC SEGREGATION OF A MATERNAL INV (10)YUNIS E; TORRES DE CABALLERO O.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 71-74; BIBL. 23 REF.Article

SERIAL DUPLICATION OF 10(Q21->Q22) IN A MENTALLY RETARDED BOY WITH CONGENITAL MALFORMATIONSKOIVISTO M; HERVA R; LINNA SL et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 224-225; BIBL. 6 REF.Article

RING CHROMOSOME 10 ASSOCIATED WITH MULTIPLE CONGENITAL MALFORMATIONSSIMONI G; ROSSELLA F; DALPRA L et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 117-121; BIBL. 8 REF.Article

IS THERE A MONOSOMY 10 QTER SYNDROME.MULCAHY MT; PEMBERTON PJ; THOMPSON E et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 1; PP. 33-35; BIBL. 3 REF.Article

MECANISMES DE FORMATION DES DUPLICATIONS: A PROPOS D'UNE OBSERVATION DE DUPLICATION 10Q22->Q25PISON H; SELE B; SALVAT J et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 137-140; ABS. ENG; BIBL. 16 REF.Article

DISTAL 10P DELETION SYNDROMEFRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 189-190; ABS. FRE; BIBL. 7 REF.Article

BALANCED TRANSMISSION OF CENTROMERIC FISSION PRODUCTS IN MANFRYNS JP; BULCKE J; HENS L et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 127-128; BIBL. 7 REF.Article

RING 10 CHROMOSOME: 46, XX, R10 (P15 Q26)SPARKES RS; LING SM; MULLER H et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 3; PP. 341-345; BIBL. 16 REF.Article

PARTIAL TRISOMY 10Q IN THREE UNRELATED PATIENTSTAYSI K; YANG V; MONAGHAN N et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 79-85; ABS. FRE; BIBL. 10 REF.Article

CHROMOSOME 10 EN ANNEAU: 46,XX,R(10) (P15Q26)SERVILLE F; BRIAULT R; TAILLEMITE JL et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 168-171; ABS. ENG; BIBL. 9 REF.Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 10RAY M; HUNTER AGW; JOSIFEK K et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 103-104; ABS. FRE; BIBL. 1 REF.Article

SERIAL DUPLICATION OF 10 (Q11->Q22) IN A PATIENT WITH MINOR CONGENITAL MALFORMATIONS.VOGEL W; BACK E; IMM W et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 2; PP. 159-163; BIBL. 15 REF.Article

THE DERMATOGLYPHIC PATTERN OF THE TRISOMY 10 P. SYNDROMERODEWALD A; STENGEL RUTKOWSKY S.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 6; PP. 330-337; BIBL. 22 REF.Article

RING CHROMOSOME 10 AND ITS CLINICAL FEATURESNAKAI H; ADACHI M; KATSUSHIMA N et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 142-144; BIBL. 5 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME NO 10.BERGER R; LARROCHE JC; TOUBAS PL et al.1977; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1977; VOL. 66; NO 5; PP. 659-662; BIBL. 8 REF.Article

PARTIAL MONOSOMY OF CHROMOSOME 10 SHORT ARMSGENCIK A; BROENNIMAN U; TOBLER R et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 107-111; BIBL. 16 REF.Article

NEW CHROMOSOMAL SYNDROMES. I: PARTIAL TRISOMY OF THE DISTAL PORTION OF THE LONG ARM OF CHROMOSOME NUMBER 10 (10Q240->10QTER): A CLINICAL ENTITYFRYNS JP; LOGGHE N; VANEYGEN M et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 2; PP. 141-143; BIBL. 18 REF.Article

PARTIAL DUPLICATION OF THE SHORT ARM OF CHROMOSOME 10: KARYOTYPE: 46, XX, DUP (10P) (PTER->P12:: P12::P12->QTER)FRYNS JP; DEROOVER J; HAEGEMAN J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 217-220; BIBL. 16 REF.Article

OCULAR PHENOTYPE IN PATIAL TRISOMY 10 Q.PROSPERI L; BERNASCONI S; FORABOSCO A et al.1977; OPHTHALMOLOGIA; SUISSE; DA. 1977; VOL. 175; NO 5; PP. 269-274; ABS. ALLEM. FR.; BIBL. 17 REF.Article

A further case of monosomy 10qterEVANS-JONES, G; WALKER, S; HOWARD, P. J et al.Clinical genetics. 1983, Vol 24, Num 3, pp 216-219, issn 0009-9163Article