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FREQUENCY AND SEGREGATION OF 16 QH+ = FREQUENCE ET SEGREGATION DE 16 QH+NIELSEN J; FRIEDRICH U; HREIDARSSON AB et al.1974; CLIN. GENET.; DANM.; DA. 1974; VOL. 5; NO 4; PP. 316-321; BIBL. 9REF.Article

PSEUDOHERMAPHRODITISM WITH CLINICAL FEATURES OF TRISOMY 18 IN AN INFANT TRISOMIC FOR PARTS OF CHROMOSOMES 16 AND 18: 47, XY, DER(18), T(16; 18) (P12; Q11) MAT.STERN LM; MURCH AR.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 3; PP. 305-307; 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

DE NOVO TRISOMY 1611->PTERDALLAPICCOLA B; CURATOLO P; BALESTRAZZI P et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 1; PP. 1-6; BIBL. 6 REF.Article

A TERMINAL LONG ARM DELETION OF CHROMOSOME 16 IN A DYSMORPHIC INFANT: 46, XY, DEL (16) (Q22)TAYSI K; FISHMAN M; SEKHON GS et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 343-347; BIBL. 4 REF.Article

THE FRAGILE SITE ON CHROMOSOME 16 (Q21Q22): DATA ON FOUR NEW FAMILIESSHABTAI F; BICHACHO S; HALBRECHT I et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 19-22; BIBL. 14 REF.Article

ERYNS SYNDROME WITHOUT DELETION 16 QCOTE GB; PAPADAKOU LAGOYANNI S; KAIRIS M et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 171-172; ABS. FRE; BIBL. 5 REF.Article

HEMOGLOBIN H DISEASE AND MENTAL RETARDATION: A NEW SYNDROME OR A REMARKABLE COINCIDENCE.WEATHERALL DJ; HIGGS DR; BUNCH C et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 305; NO 11; PP. 607-612; BIBL. 20 REF.Article

MONOSOMY 10 QTER DUE TO A BALANCED FAMILIAL TRANSLOCATION: T(10; 16) (Q 25.2; Q24)WEGNER RD; KUNZE J; PAUST H et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 2; PP. 130-133; BIBL. 5 REF.Article

PARTIAL TRISOMY FOR LONG ARM OF CHROMOSOME 16BUCKTON KE; BARR DGD.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 6; PP. 483; BIBL. 3 REF.Article

BALANCED RECIPROCAL TRANSLOCATION T(1;16) (Q12;Q11) IN TWO GENERATIONS OF A FAMILYESSER KJ; HABEDANK M.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 1; PP. 92; BIBL. 2 REF.Article

A CULTURE WITH A DERIVATIVE CHROMOSOME 10 FROM A PATERNAL (10;16) TRANSLOCATION. REPOSITORY IDENTIFICATION NO 6M-139B.EMANUEL B; ZACKAI EH; HELLMAN WJ et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 19; NO 4; PP. 240Article

HETEROCHROMATIC REGIONS ON CHROMOSOMES 1,9, 16, AND Y IN CHILDREN WITH SOME DISTURBANCES OCCURING DURING EMBRYO DEVELOPMENTPODUGOLNIKOVA OA; BLUMINA MG.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 2; PP. 183-188; BIBL. 28 REF.Article

ANTIKOERPERMANGELSYNDROM UND CHROMOSOMENANOMALIEN. = SYNDROME DE DEFICIT EN ANTICORPS ET ANOMALIES CHROMOSOMIQUESWIERSBITZKY S; SCHROETER C.1976; ALLERGIE U. IMMUNOL.; DTSCH.; DA. 1976; VOL. 22; NO 2; PP. 167-170; ABS. ANGL.; BIBL. 28 REF.Article

HETEROCHROMATIN BLOCKS OF CHROMOSOME PAIRS 1, 9 AND 16 AS A "MARKER" FOR HUMAN DIPLOID CELLS WI-38.GARZICIC B; KESEROVIC B; KESEROVIC N et al.1976; J. BIOL. STANDARDIZ.; G.B.; DA. 1976; VOL. 4; NO 4; PP. 367-369; H.T. 1; BIBL. 7 REF.Article

TERTIARY TRISOMY 47,XX,+14Q-, RESULTING FROM MATERNAL BALANCED TRANSLOCATION, 46,XX,T (14;16) (Q11;Q24).YOUNG SR; DONOVAN DM; GREER HA et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 331-334; BIBL. 11 REF.Article

SINDROME DE TRISOMIA 8 CON DUPLICACION DE HETERO-CROMATINA EN CROMOSOMA 16. = SYNDROME DE TRISOMIE 8 AVEC DUPLICATION DE L'HETEROCHROMATINE DANS LE CHROMOSOME 16PRIETO F; BADIA L; TABOADA D et al.1977; REV. ESP. PEDIATR.; ESP.; DA. 1977; VOL. 33; NO 194; PP. 177-186; ABS. ANGL.; BIBL. 18 REF.Article

CYTOMEGALOVIRUS AND PENTA X SYNDROME = VIRUS CYTOMEGALIQUE ET SYNDROME PENTA XGENOUD J; GUIBAUD P; BETHENOD M et al.1974; J. PEDIATR.; U.S.A.; DA. 1974; VOL. 85; NO 6; PP. 869; BIBL. 3REF.Article

BALANCIERTE TRANSLOKATION RCP (3P+ 16Q-) BEI EINER MUTTER ALS MOEGLICHE URSACHE MULTIPLER TOTODER FRUEHGEBURTEN. = UNE TRANSLOCATION BALANCEE (3P+; 16Q-) CHEZ LA MERE, COMME CAUSE LA PLUS PROBABLE DE PLUSIEURS ENFANTS MORTS-NES OU PREMATURESKIM MA; MAJEWSKI F; HABERLANDT WF et al.1974; ARCH. GENET.; SCHWEIZ; DA. 1974; VOL. 47; NO 3; PP. 129-135; ABS. ANGL.; BIBL. 9 REF.Article

Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band regionELDER, F. F. B; FERGUSON, J. W; LOCKHART, L. H et al.Human genetics. 1984, Vol 67, Num 2, pp 233-236, issn 0340-6717Article

Interstidial deletion for a region in the long arm of chromosome 16LIN, C. C; LOWRY, R. B; SNYDER, F. F et al.Human genetics. 1983, Vol 65, Num 2, pp 134-138, issn 0340-6717Article

Partial trisomy 16 q in two boys resulting from a maternal translocation, t(15; 16) (p12; q11)NEVIN, N. C; COFFEY, W. W; NEVIN, J et al.Clinical genetics. 1983, Vol 24, Num 5, pp 375-379, issn 0009-9163Article

Etude cytogénétique d'un cas de translocation balancée de novo des chromosomes 12 et 16CHENG ZAIYU; LIU CHUNYUN; GAO CHUNSHENG et al.Yíchuán xuébào. 1983, Vol 10, Num 5, pp 419-422, issn 0379-4172Article

An audit trisomy 16 in manWOLSTENHOLME, J.Prenatal diagnosis. 1995, Vol 15, Num 2, pp 109-121, issn 0197-3851Article

Interstitial deletion of chromosome 16q : 16q22 is critical for 16q- syndromeFUJIWARA, M; YOSHIMOTO, T; MORITA, Y et al.American journal of medical genetics. 1992, Vol 43, Num 3, pp 561-564, issn 0148-7299Article

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