kw.\*:("C9 CHROMOSOME")
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EXPRESSION OF GALT IN TWO UNRELATED 9P - PATIENTS. EVIDENCE FOR ASSIGNMENT OF THE GALT LOCUS TO THE 9P21 BANDBRICARELLI FD; MAGNANI M; ARSLANIAN A et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 112-114; BIBL. 19 REF.Article
THE TRISOMY 9 SYNDROMECARPENTER BF; TOMKINS DJ.1982; PERSPECTIVES IN PEDIATRIC PATHOLOGY; ISSN 0091-2921; USA; DA. 1982; VOL. 7; PP. 109-120; BIBL. 43 REF.Article
POLYMORPHISM OF CHROMOSOME 9 IN 600 GREEK SUBJECTS.METAXOTOU C; KALPINI MAVROU A; PANAGOU M et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 30; NO 1; PP. 85-89; BIBL. 13 REF.Article
PERICENTRIC INVERSION, INV (9) (P22 Q32), IN THE FATHER OF A CHILD WITH A DUPLICATION-DELETION OF CHROMOSOME 9 AND GENE DOSAGE EFFECT FOR ADENYLATE KINASE-1MATTEI JF; MATTEI MG; ARDISSONE JP et al.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 2; PP. 129-136; BIBL. 13 REF.Article
REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF CHROMOSOME 9KHAN PM; ROBSON EB.1978; CYTOGENET. CELL GENET.; CHE; DA. 1978; VOL. 22; NO 1-6; PP. 106-110; BIBL. 2 P.Conference Paper
Tetrasomy 9p confirmed by GALTBALESTRAZZI, P; CROCI, G; FRASSI, C et al.Journal of medical genetics. 1983, Vol 20, Num 5, pp 396-399, issn 0022-2593Article
L'INSTABILITE PSYCHO-MOTRICE EST-ELLE VRAIMENT UN SIGNE CARACTERISTIQUE DE LA TRISOMIE 9P.: A PROPOS DE 3 OBSERVATIONSLE MAREC B; BOUCHARD C; BOIXEL J et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 263-269; ABS. ENG; BIBL. 8 REF.Article
TRISOMY 9 SYNDROMEANNEREN G; SEDIN G.1981; ACTA PAEDIATR. SCAND.; ISSN 0001-656X; SWE; DA. 1981; VOL. 70; NO 1; PP. 125-128; BIBL. 17 REF.Article
EXPRESSION OF GALT IN 9P CHROMOSOME ALTERATIONS: ASSIGNMENT OF GALT LOCUS TO 9CEN->9P22SPARKES RS; SPARKES MC; FUNDERBURK SJ et al.1980; ANN. HUM. GENET.; GBR; DA. 1980; VOL. 43; NO 4; PP. 343-347; BIBL. 8 REF.Article
CHROMOSOMAL VARIANTS AND NONDISJUNCTION.FORD JH; LESTER P.1978; CYTOGENET. CELL. GENET.; CHE; DA. 1978; VOL. 21; NO 5; PP. 300-303; BIBL. 10 REF.Article
PROBABLE LINKAGE BETWEEN THE HUMAN GALACTOSE-1-P URIDYL TRANSFERASE LOCUS AND 9QHSPARKES RS; EPSTEIN PA; KIDD KK et al.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 2; PP. 188-193; BIBL. 29 REF.Article
DELTA -AMINOLEVULINATEDEHYDRASE: SYNTENY WITH ABO-AK1-ORM (AND ASSIGNMENT TO CHROMOSOME 9)EIBERG H; MOHR J; NIELSEN LS et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 2; PP. 150-154; BIBL. 5 REF.Article
CHIASMA DERIVED GENETIC LENGHTS AND RECOMBINATION FRACTIONS: CHROMOSOMES 2 AND 9LAURIE DA; PALMER RW; HULTEN MA et al.1982; ANNALS OF HUMAN GENETICS; ISSN 0003-4800; GBR; DA. 1982; VOL. 46; NO 3; PP. 233-244; BIBL. 8 REF.Article
UNE NOUVELLE OBSERVATION DE CHROMOSOME 9 EN ANNEAUPORTNOL MF; VAN DEN AKKER J; LE PORRIER N et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 164-167; ABS. ENG; BIBL. 12 REF.Article
UNE NOUVELLE OBSERVATION DE CHROMOSOME 9 EN ANNEAUPORTINOI MF; VAN DEN AKKER J; LE PORRIER N et al.1983; SEMAINE DES HOPITAUX; ISSN 0037-1777; FRA; DA. 1983; VOL. 59; NO 3; PP. 185-188; ABS. ENG; BIBL. 12 REF.Article
TWO UNUSUAL G-BAND VARIANTS OF THE PHORT ARM OF CHROMOSOME 9SUTHERLAND GR; EYRE H.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 5; PP. 331-334; BIBL. 7 REF.Article
COMPLETE TRISOMY 9 IN TWO LIVEBORN INFANTSMANTAGOS S; MCREYNOLDS JW; SEASHORE MR et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 377-382; BIBL. 19 REF.Article
LEUKOCYTE AND FIBROBLAST INTERFERON GENES ARE LOCATED ON HUMAN CHROMOSOME 9OWERBACH D; RUTTER WJ; SHOWS TW et al.1981; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 5; PP. 3123-3127; BIBL. 50 REF.Article
WHERE IS THE GENE FOR GALTMULCAHY MT; WILSON RG.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 129-130; BIBL. 15 REF.Article
COMPLETE DEFICIENCY OF CONSTITUTIVE HETEROCHROMATIN ON A HUMAN CHROMOSOME 9BUYS CHCM; YPMA JMM; GOUW WL et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 129-132; BIBL. 8 REF.Article
MODERATE MENTAL RETARDATION AND NONSPECIFIC DYSMORPHIC SYNDROME ASSOCIATED WITH RING CHROMOSOME 9FRYNS JP; LAMBRECHTS A; JANSSEUNE H et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 29-32; BIBL. 15 REF.Article
Non C-banding variants in some normal families might be homogeneously staining regionsWEBB, G. C; KRUMINS, E. J. M; EICHENBAUM, S. Z et al.Human genetics. 1989, Vol 82, Num 1, pp 59-62, issn 0340-6717, 4 p.Article
MAPPING AK1, ACONS, AND AK3 TO CHROMOSOME 9 IN MAN EMPLOYING AN X/9 TRANSLOCATION AND SOMATIC CELL HYBRIDS.SHOWS TB; BROWN JA.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 19; NO 1; PP. 26-37; BIBL. 2 P. 1/2Article
REGIONAL ASSIGNMENTS OF THE LOCI AK3, ACON5, AND ASS ON HUMAN CHROMOSOME 9CARRITT B; POVEY S.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 23; NO 3; PP. 171-181; BIBL. 29 REF.Article
FAMILY STUDIES WITH THE CHROMOSOME 9 MARKERS ABO, AK1, ACONS AND 9QH.ROBSON EB; COOK PJL; BUCKTON KE et al.1977; ANN. HUM. GENET.; G.B.; DA. 1977; VOL. 41; NO 1; PP. 53-60; BIBL. 27 REF.Article