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Results 1 to 25 of 735

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ORIGIN OF A SMALL METACENTRIC CHROMOSOME: FAMILIAL AND CYTOGENETIC EVIDENCE = ORIGINE D'UN PETIT CHROMOSOME METACENTRIQUE: PREUVE FAMILIALE CYTOGENETIQUETAYLOR KM; WOLFINGER HL; BROWN MG et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 364-369; BIBL. 11 REF.Article

CYTOGENETICS OF 50 PATIENTS WITH MENTAL RETARDATION AND MULTIPLE CONGENITAL ANOMALIES AND 50 NORMAL SUBJECTS. MADISON BLIND STUDY IVMAGNELLI NC.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 2; PP. 169-182; BIBL. 23 REF.Article

TRISOMIE 4P DE NOVO PAR ISOCHROMOSOME 4P.ANDRE MJ; AURIAS A; DE BERRANGER P et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 2; PP. 127-131; ABS. ANGL.; BIBL. 16 REF.Article

ETUDE CYTOGENETIQUE DE LA MALADIE DU CRI DU CHAT. A PROPOS D'UNE FAMILLE OU TROIS ENFANTS SONT ATTEINTS DE L'AFFECTION ET UN DE SA RECIPROQUEBOUVIER G.1974; LYON; ASSOC. CORP. ETUD. MED. LYON; DA. 1974; PP. 1-62; BIBL. 19P.; (THESE DOCT. MED.; CLAUDE-BERNARD LYON)Thesis

IDENTIFICATION DE DEUX TRANSLOCATIONS FAMILIALESLAURENT C; BIEMONT MC; ROBERT JM et al.1974; SEM. HOP., ANN. GENET.; FR.; DA. 1974; VOL. 17; NO 4; PP. 279-281; ABS. ANGL.; BIBL. 8REF.Serial Issue

TYPE AND CONTRETYPE SIGNS IN MONOSOMY AND TRISOMY 9P: ON A CASE 46,XY,DEL(9) (PTER->P12:)HERNANDEZ A; RIVERA H; JIMENEZ SAINZ M et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 155-157; ABS. FRE; BIBL. 13 REF.Article

AN UNUSUAL CHROMOSOMAL SEGREGATION IN A FAMILY WITH A TRANSLOCATION BETWEEN CHROMOSOMES 3 AND 12 = SEGREGATION CHROMOSOMIQUE INHABITUELLE DANS UNE FAMILLE CONDUCTRICE D'UNE TRANSLOCATION ENTRE LES CHROMOSOMES 3 ET 12SACHDEVA S; SMITH GF; JUSTICE P et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 303-305; BIBL. 4 REF.Article

Detection of microdeletions in the short arm of the X chromosome by chromosome stretchingKUECHLER, A; MUELLER, C. R; LIEHR, T et al.Cytogenetics and cell genetics. 2001, Vol 95, Num 1-2, pp 12-16, issn 0301-0171Article

ARE NORS EASILY TRANSLOCATED TO DELETED CHROMOSOMES.ZANKL H; HUWER H.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 42; NO 2; PP. 137-142; BIBL. 22 REF.Article

POSSIBLE INTRACHROMOSOMAL DUPLICATION IN A CASE OF TRISOMY 9 P.CHIYO H; FURUYAMA J; SUEHARA N et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 2; PP. 217-221; BIBL. 15 REF.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

CARYOTYPE 45,XY-18-21, +T(18;21) (18 Q TER->CEN->21 Q TER) CHEZ UN NOURRISSON.SERVILLE F; FONTAN D; BROUSTET A et al.1977; BORDEAUX MED.; FR.; DA. 1977; VOL. 10; NO 18; PP. 1227-1230; BIBL. 4 REF.Article

DUE CASI DI SINDROME 18P-ED UN CASO DI TRISOMIA 18P IN UNA STESSA FRATRIA. = DEUX CAS DE SYNDROME 18P- ET UN CAS DE TRISOMIE 18P DANS UNE MEME FRATRIEROSANO M; DE SALAZAR E; BRINCHI V et al.1977; NEUROPSICHIATR. INFANT.; ITAL.; DA. 1977; NO 197; PP. 1221-1237; ABS. ANGL.; BIBL. 3 P. 1/2Article

RDNA AND ACROCENTRIC CHROMOSOMES IN MAN. I. RDNA LEVELS IN A SUBJECT CARRIER OF A 8P/13P BALANCED TRANSLOCATION AND IN HIS UNBALANCED SON.GUANTI G; MOLLICA G; POLIMENO L et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 103-107; BIBL. 10 REF.Article

PTER->12P 12.2: POSSIBLE ASSIGNMENT OF HUMAN TRIOSE PHOSPHATE ISOMERASE.RETHORE MO; KAPLAN JC; JUNEN C et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 2; PP. 235-237; BIBL. 8 REF.Article

AUGMENTATION DE L'ACTIVITE DE LA LDH-B CHEZ UN GARCON TRISOMIQUE 12P PAR MALSEGREGATION D'UNE TRANSLOCATION MATERNELLE T(12;14)(Q12;P11)RETHORE MO; KAPLAN JC; JUNIEN C et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 81-87; ABS. ANGL.; BIBL. 15REF.Article

FREQUENCY OF DELETION OF SHORT ARM SATELLITES IN ACROCENTRIC CHROMOSOMES = FREQUENCE DE LA DELETION DES SATELLITES DES BRAS COURTS DES CHROMOSOMES ACROCENTRIQUESNIELSEN J; FRIEDRICH U; HREIDARSSON AB et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 2; PP. 177-180; BIBL. 16REF.Article

TRISOMY OF THE SHORT ARM OF CHROMOSOME 17 = TRISOMIE DU BRAS COURT DU CHROMOSOME 17LATTA E; HOO JJ.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 23; NO 3; PP. 213-217; ABS. ALLEM.; BIBL. 9REF.Article

TRANSLOCATION T(2;14) EQUILIBREE CHEZ UNE MERE ET TRISOMIE PARTIELLE D'UNE PARTIE DU BRAS COURT D'UN CHROMOSOME NO2 CHEZ DEUX DE SES ENFANTSSTOLL C; MESSER J; VORS J et al.1974; SEM. HOP., ANN. GENET.; FR.; DA. 1974; VOL. 17; NO 3; PP. 193-196; ABS. ANGL.; BIBL. 6 REF.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

UNE OBSERVATION DE DELETION PARTIELLE DU BRAS COURT DU CHROMOSOME 12. LOCALISATION DU GENE DE LA LACTICO DESHYDROGENASEBMALPUECH G; KAPLAN JC; RETHORE MO et al.1975; LYON MED.; FR.; DA. 1975; VOL. 233; NO 3; PP. 275-279; ABS. ANGL.; BIBL. 10REF.Article

STRUCTURAL ABERRATIONS OF CHROMOSOME 18. I. THE 18P- SYNDROMESCHINZEL A; SCHMID W; LUSCHER U et al.1974; ARCH. GENET.; SCHWEIZ; DA. 1974; VOL. 47; NO 1; PP. 1-15; ABS. ALLEM.; BIBL. 3P.1/2Article

SINDROME DE MAULLIDO DE GATO. ESTUDIO COMPARATIVO EN EDADES DISTINTAS = SYNDROME DU CRI DU CHAT. ETUDE COMPARATIVE A DIVERS AGESANSEDE A; NOYA M; NOGUEIRA CAAMANO L et al.1974; MED. CLIN.; ESP.; DA. 1974; VOL. 63; NO 10; PP. 509-516; ABS. ANGL.; BIBL. 1P.1/2Article

DELETION OF THE SHORT ARM OF CHROMOSOME #9 (46, 9P-): A NEW DELETION SYNDROMEALFI O; DONNELL GN; CRANDALL BF et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 17-22; ABS. FR.; BIBL. 19REF.Serial Issue

A CASE OF THE 18P-SYNDROMESUBRT I; BERANKOVA J.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 16; NO 4; PP. 359-360Serial Issue

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