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CHROMOSOME Y ET FILIATION PATERNELLE. ANALYSE DE TROIS ETUDES FAMILIALES AVEC TRANSMISSION HEREDITAIRE D'UNE ANOMALIE OU D'UNE VARIANTE DE L'YBENEZECH M; NOEL B; TACHOIRES M et al.1976; BORDEAUX MED.; FR.; DA. 1976; VOL. 9; NO 3; PP. 197Article

A(Y; 15) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-118HAHNENMANN N; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 408-409Article

UN CAS DE CHROMOSOME Y ANORMALEMENT LONG CHEZ BOS TAURUS L.CRIBIU EP; POPESCU CP.1974; ANN. GENET. SELECT. ANIMALE; FR.; DA. 1974; VOL. 6; NO 3; PP. 387-390; ABS. ANGL.; BIBL. 9REF.Article

IDENTIFICAZIONE DEL CROMOSOMA Y E DELLE SUE ANOMALIE MEDIANTE FLUORESCENZA INDOTTA = IDENTIFICATION DU CHROMOSOME Y ET DE SES ANOMALIES PAR FLUORESCENCE PROVOQUEESANDRUCCI M; FABRIS C; BOGETTI G et al.1974; MINERVA PEDIATR.; ITAL.; DA. 1974; VOL. 26; NO 21; PP. 1104-1111; BIBL. 13REF.Article

Tow cases of prenatal diagnosis of a stallited Yq chromosomeBAYLESS-UNDERWOOD, L; SECHIN CHO; WARD, B et al.Clinical genetics. 1983, Vol 24, Num 5, pp 359-364, issn 0009-9163Article

A BOY WITH 46, X, DEL (Y) DUE TO A DE NOVO MUTATIONFRIED K; ROSENBLATT M; VARSANO D et al.1975; HUM. HERED.; SWITZ.; DA. 1975; VOL. 25; NO 6; PP. 472-476; BIBL. 3 REF.Article

PRENATAL CYTOGENETIC ANALYSIS OF WOMEN WITH HIGH RISK FOR GENETIC DISORDERSRARY JM; PARK IJ; HELLER RH et al.1974; J. HERED.; U.S.A.; DA. 1974; VOL. 65; NO 4; PP. 209-212; BIBL. 18REF.Article

CHROMOSOME Y LONG (YQ+) ET COMPORTEMENT DELICTUEUX. ETAT ACTUEL DE NOS CONNAISSANCESBENEZECH M; NOEL B; MANELPHE C et al.1975; ANN. MEDICO-PSYCHOL.; FR.; DA. 1975; VOL. 2; NO 2; PP. 313-321; BIBL. 1 P. 1/2Article

LE CHROMOSOME YPIERSON M; GILGENKRANTZ S; SABORIO M et al.1975; J. MED. STRASBOURG; FR.; DA. 1975; VOL. 6; NO 7-8; PP. 433-436; ABS. ANGL.; BIBL. 1 REF.Article

DYSGENESIE GONADIQUE ET CHROMOSOME Y DICENTRIQUE. A PROPOS DE DEUX OBSERVATIONSGIRAUD F; MATTEI JF; MATTEI MG et al.1976; PEDIATRIE; FR.; DA. 1976; VOL. 31; NO 1; PP. 90-91; (SOC. FR. PEDIATR. REUN. PEDIATR. SUD FRANCE; CLERMONT FERRAND; 1975)Conference Paper

PRENATAL EVALUATION IN A CASE OF FAMILIAL Y CHROMOSOME LONG ARM DELETION (YQ-) = EVALUATION ANTENATALE DANS UN CAS DE DELETION FAMILIALE DU BRAS LONG DU CHROMOSOMEY (YQ-)MACINTYRE MN; RUSTAD RC; BOERGER TURK K et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 367-370; BIBL. 15REF.Article

45, X/46, XXQ DIC-GESCHLECHTSCHROMOSOMENMOSAIK = MOSAIQUE CHROMOSOMIQUE SEXUELLE 45, X/46, XYQ DICFREY RO; BUHLER EM; BUHLER UK et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 2; PP. 81-90; ABS. ANGL.; BIBL. 1 P.Article

ETUDE MEIOTIQUE ET MITOTIQUE DANS UN CAS DE TRANSLOCATION T (5;Y).DUTRILLAUX B; GUEGUEN J.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 241-245; ABS. ANGL.; BIBL. 13 REF.Article

FOUR NEW CASES OF DICENTRIC Y CHROMOSOMES.GIRAUD F; MATTEI JF; LUCAS C et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 3; PP. 249-260; BIBL. 1 P. 1/2Article

A NEW TYPE OF INVERSION OF A HUMAN Y CHROMOSOME. = UN NOUVEAU TYPE D'INVERSION DANS LE CHROMOSOME Y CHEZ L'HOMMESOFUNI T; TANABE K; NARUTO J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 2; PP. 91-97; BIBL. 1 P. 1/2Article

TURNER'S SYNDROME AND 46,X,I(YQ) KARYOTYPE = SYNDROME DE TURNER ET CARYOTYPE 46,X,I(YQ)MAGNELLI NC; VIANNA MORGANTE AM; FROTA PESSOA O et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 403-406; BIBL. 5REF.Article

INDICAZIONE PER L'INTERPRETAZIONE DELLE VARIANTI NORMALI E PATOLOGICHE DEL CROMOSOMA Y. = INDICATIONS POUR L'INTERPRETATION DES VARIANTES NORMALES ET PATHOLOGIQUES DU CHROMOSOME YVIANELLO MG; BONIOLI E; FRESCHI F et al.1977; MINERVA PEDIATR.; ITAL.; DA. 1977; VOL. 29; NO 18; PP. 1201-1206; ABS. ANGL.; BIBL. 1 P. 1/2Article

Cytogenetic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y;13) translocation showing differential centromeric activityING, P. S; SMITH, S. D.Clinical genetics. 1983, Vol 24, Num 3, pp 194-199, issn 0009-9163Article

A NEW CASE OF SATELLITED YQ CHROMOSOMEMARTIN MJ; RODRIGUEZ T; ABRISQUETA JA et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 3; PP. 277Article

A NEW CASE OF HUMAN Y CHROMOSOME WITH SATELLITES ON THE LONG ARMSTELLA M; ROSSI R; BONFANTE A et al.1980; J. GENET. HUM.; CHE; DA. 1980; VOL. 28; NO 1; PP. 39-45; ABS. FRE; BIBL. 16 REF.Article

NONMOSAIC H6, X, R(Y) KARYOTYPE WITH FEMALE PHENOTYPE.LASZLO J; GAAL M; BOSZE P et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 3; PP. 351-356; BIBL. 16 REF.Article

AN XX MALE WITH A 46,XX/47,XX+Y(Q12->QTER) KARYOTYPEMIRO R; CABALLIN MR; COLL MD et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 82-84; BIBL. 22 REF.Article

TOOTH SIZES IN TWO MALES WITH DELETIONS OF THE LONG ARM OF THE Y-CHROMOSOMEALVESALO L; DE LA CHAPELLE A.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; NO 1; PP. 49-54; BIBL. 2 P.Article

UNSTABLE RING Y CHROMOSOME IN AN ASPERMIC MALESTEINBACH P; FABRY H; SCHOLZ W et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 3; PP. 227-231; BIBL. 20 REF.Article