DUPLICATION 3 P SYNDROME: REPORT OF A NEW CASE AND REVIEW OF THE LITERATURECHARROW J; COHEN MM; MEEKER D et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 4; PP. 431-436; BIBL. 16 REF.Article

FAMILIAL PARTIAL DISTAL 18Q (18Q22-18Q23) TRISOMYDE MUELENAERE A; FRYNS JP; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 184-186; ABS. FRE; BIBL. 4 REF.Article

PARTIAL DISTAL 1 Q TRISOMY. A DISTINCT CLINICAL DYSMORPHIC SYNDROME IN ADULTHOODFRYNS JP; DE MUELENAERE A; PEDERSEN J et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 181-182; ABS. FRE; BIBL. 7 REF.Article

TRISOMY 18 Q-. TRISOMY MAPPING OF CHROMOSOME 18 REVISITEDTURLEAU C; CHAVIN COLIN F; NARBOUTON R et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 1; PP. 20-26; BIBL. 11 REF.Article

GAMMOPATIA MONOCLONALE IDIOPATICA E ANOMALIE CROMOSOMICHE = GAMMOPATHIE MONOCLONALE IDIOPATHIQUE ET ANOMALIES CHROMOSOMIQUESCATENA R; GAMBETTI M.1980; PATHOLOGICA; ISSN 0031-2983; ITA; DA. 1980; VOL. 72; NO 1018; PP. 235-241; ABS. ENG; BIBL. 12 REF.Article

AGENESIS OF THE LUNG ASSOCIATED WITH A CHROMOSOME ABNORMALITY (46,XX,2P+)SAY B; CARPENTER NJ; GIACOIA G et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 6; PP. 477-478; BIBL. 6 REF.Article

PARTIAL TRISOMY 12QZABEL B; BAUMANN W.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 2; PP. 144-146; BIBL. 2 REF.Article

STRUCTURAL ABERRATION OF THE X CHROMOSOME IN A PATIENT WITH GONADAL DYSGENESIS: AN APPROACH TO KARYOTYPE-PHENOTYPE CORRELATIONVARELLA GARCIA M; TAJARA EH; TOLEDO GAGLIARDI AR et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 3; PP. 228-231; BIBL. 11 REF.Article

TRISOMY 22 SYNDROME IN A 26-YEAR-OLD FEMALE: A FOLLOW-UP EXAMINATIONANNEREN G; GUSTAVSON KH.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 94; NO 1; PP. 67-71; BIBL. 10 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

ABNORMALITY OF CHROMOSOME 16 AND ITS PHENOTYPIC EXPRESSIONGOLDEN NL; BILENKER R; JOHNSON WE et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 1; PP. 41-45; BIBL. 8 REF.Article

PARTIAL TRISOMIE 5Q: THREE DIFFERENT PHENOTYPES DEPENDING ON DIFFERENT DUPLICATION SEGMENTSRODEWALD A; ZANKL M; GLEY EO et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 2; PP. 191-198; BIBL. 8 REF.Article

DE NOVO DUPLICATION 1Q32-Q42: VARIABILITY OF PHENOTYPIC FEATURES IN PARTIAL 1Q TRISOMICSLUNGAROTTI MS; FALORNI A; CALABRO A et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 398-402; BIBL. 27 REF.Article

PARTIAL TRISOMY 6Q, DUE TO BALANCED MATERNAL TRANSLOCATION (6; 22) (Q21; P13) OR (Q21; PTER)STAMBERG J; SHAPIRO J; VALLE D et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 2; PP. 122-125; BIBL. 5 REF.Article

TWO FAMILIAL CASES OF TRISOMY 15Q DIST DUE TO A RCP (5; 15) (P14; Q21)TZANCHEVA M; KRACHOUNOVA M; DAMJANOVA Z et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 275-277; BIBL. 5 REF.Article

DUPLICATION 12Q MOSAICISM IN TWO UNRELATED PATIENTS WITH A SIMILAR SYNDROMEHARROD MJE; BYRNE JY; DEV VG et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 2; PP. 123-129; BIBL. 4 REF.Article

PARTIAL 3Q TRISOMY DUE TO AN UNBALANCED 3/10 TRANSLOCATIONBLUMBERG B; MOORE R; MOHANDAS T et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 3; PP. 335-339Article

PARTIAL TRISOMY 1(Q42->TER)LEISTI J; AULA P.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 5; PP. 371-378; BIBL. 8 REF.Article

DOWN'S SYNDROME ASSOCIATED WITH FAMILIAL 21P+ VARIANTKLECZKOWSKA A; KUBIEN E.1981; GENET. POL.; ISSN 0016-6715; POL; DA. 1981; VOL. 22; NO 1; PP. 113-115; ABS. POL/RUS; BIBL. 11 REF.Article

EVIDENCE OF GENE DOSAGE EFFECT FOR HK1 IN THE RED CELLS OF A PATIENT WITH TRISOMY 10PTER->P 13DALLA PICCOLA B; SERENA LUNGAROTTI M; MAGNANI M et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 45-47; ABS. FRE; BIBL. 11 REF.Article

NEW CHROMOSOMAL DYSMORPHIC SYNDROMES. IV: TRISOMY 12PSTENGEL RUTKOWSKI S; ALBERT A; MURKEN JD et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 136; NO 3; PP. 249-262; BIBL. 33 REF.Article

TRIPLEX GENE DOSAGE EFFECT FOR BETA -GLUCURONIDASE AND POSSIBLE ASSIGNMENT TO BAND Q22 IN A PARTIAL DUPLICATION 7QDANESINO C; GIMELLI G; CUOCO C et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 371-373; BIBL. 9 REF.Article

TRISOMY 18Q. A CASE REPORT AND REVIEW OF KARYOTYPE-PHENOTYPE CORRELATIONSMATSUOKA R; MATSUYAMA S; YAMAMOTO Y et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 78-82; BIBL. 18 REF.Article

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

Duplicación parcial del cromosoma 4q (q31, q35) : síndrome aurículo-acro-renal = PARTIAL DUPLICATION OF CHROMOSOME 4Q (Q31, Q35) : AURICULO-ACRO-RENAL SYNDROMECARRASCOSA ROMERO, M; GARCIA MIALDEA, O; COMPANY, A. Vidal et al.Anales de pediatria (2003. Ed. impresa). 2008, Vol 68, Num 4, pp 361-364, issn 1695-4033, 4 p.Article