CYTOGENETIC ANALYSIS IN HUMAN BONE MARROW TRANSPLANTATIONSPARKES RS.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 4; PP. 345-352; BIBL. 32 REF.Article

PARTIAL TRISOMY OF 13 (PTER->Q12) DUE TO 47, XY,+DER (13), T(13; 22) (Q12; Q13)MATMOEDJONO SJ; SPARKES RS.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 241-246; BIBL. 19 REF.Article

EXPRESSION OF DIFFERENTIATED FUNCTIONS IN HEPATOMA CELL HYBRIDS: ALANINE AMINOTRANSFERASE = EXPRESSION DE FONCTIONS DIFFERENCEES DANS LES HYBRIDES DE CELLULES D'HEPATOMES: ALANINE AMINOTRANSFERASESPARKES RS; WEISS MC.1973; PROC. NATION. HCAD. SCI. U.S.A.; U.S.A.; DA. 1973; VOL. 70; NO 2; PP. 377-381; BIBL. 15REF.Serial Issue

ABNORMAL CEREBRAL CORTICAL CONVOLUTIONS IN AN XYY FETUSAUSTIN GE; SPARKES RS.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 2; PP. 173-175; BIBL. 12 REF.Article

RING 14 CHROMOSOME: ASSOCIATION WITH SEIZURESLIPPE BM; SPARKES RS.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 4; PP. 301-305; BIBL. 11 REF.Article

RING CHROMOSOME 16NEIDENGARD L; SPARKES RS.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 175-177; BIBL. 11 REF.Article

TWO BALANCED TRANSLOCATIONS IN THREE GENERATIONS OF A PEDIGREE: T(7;10)(Q11;Q22) AND T(14;21)(14QTER->CEN->21QTER)BASS HN; SPARKES RS.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 3; PP. 215-218; BIBL. 7 REF.Article

PURE GONADAL DYSGENESIS WITH NONMOSAIC XY SEX CHROMOSOMES.MELDRUM DR; SPARKES RS.1976; OBSTETR. AND GYNECOL.; U.S.A.; DA. 1976; VOL. 48; NO 3; PP. 357-359; BIBL. 11 REF.Article

THYMIDINE KINASE ACTIVITY AND HUMAN CHROMOSOME NO. 18.CRANDALL BF; SPARKES RS.1971; BIOCHEM. GENET.; U.S.A.; DA. 1971; VOL. 5; NO 5; PP. 451-456; BIBL. 16REF.Serial Issue

TRISOMY E (18) SYNDROME: CLINICAL SPECTRUM IN 12 NEW CASES, INCLUDING CHROMOSOME AUTORADIOGRAPHY IN 4 = SYNDROME DE TRISOMIE E (18): ANALYSE CLINIQUE DANS 12 NOUVEAUX CAS AVEC AUTORADIOGRAPHIE DES CHROMOSOMES DANS 4 CASWEBER FM; SPARKES RS.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 363-366; BIBL. 14 REF.Serial Issue

AN XXXY BOY WITH X/XY HALF-SISTERWELCH MJ; SPARKES RS.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 3; PP. 181-187; BIBL. 17 REF.Article

FAMILIAL PERICENTRIC INVERSION OF CHROMOSOME 8: IS BREAKPOINT P22Q23 IMPORTANT IN THE FORMATION OF UNBALANCED RECOMBINANTSMOEDJONO SJ; SPARKES RS.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 4; PP. 235-237; ABS. FRE; BIBL. 6 REF.Article

THE PROBLEM OF PARTIAL TRISOMY 22 RECONSIDEREDFELDMAN GM; SPARKES RS.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 1; PP. 97-101; BIBL. 10 REF.Article

INHERITED 13:14 TRANSLOCATION AND METACENTRIC MICROCHROMOSOME ASSOCIATED WITH TRISOMY 21: REPORT OF 2 CASESLEDDET CHEVALIER I; SPARKES RS.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 5; PP. 386-390; BIBL. 21 REF.Article

Q(Q23->QTER) DUPLICATION: GOTS, HK1, AND OTHER GENE MARKERS.SPARKES RS; BASS; SPARKES MC et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 267-270; BIBL. 6 REF.Article

THE HUMAN PHOSPHOSERINE PHOSPHATASE GENE (PSP) IS MAPPED TO CHROMOSOME 7 BY SOMATIC CELL GENETIC ANALYSISSPARKES RS; MOHANDAS T; SPARKES MC et al.1983; CYTOGENETICS AND CELL GENETICS; ISSN 0301-0171; CHE; DA. 1983; VOL. 35; NO 1; PP. 70-71; BIBL. 7 REF.Article

TANGIER DISEASE: HETEROZYGOTE DETECTION AND LINKAGE ANALYSISSUAREZ BK; SCHONFELD G; SPARKES RS et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 150-156; BIBL. 36 REF.Article

REACTIVATION OF AN INACTIVE HUMAN X CHROMOSOME: EVIDENCE FOR X INACTIVATION BY DNA METHYLATIONMOHANDAS T; SPARKES RS; SHAPIRO LJ et al.1981; SCIENCE; ISSN 0036-8075; USA; DA. 1981; VOL. 211; NO 4480; PP. 393-396; BIBL. 25 REF.Article

TETRASOMY 9P: CONFIRMATION BY ENZYME ANALYSISMOEDJONO SJ; CRANDALL BF; SPARKES RS et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 3; PP. 227-230; BIBL. 8 REF.Article

THE 9P-SYNDROMEFUNDERBURK SJ; SPARKES RS; KLISAK I et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 1; PP. 75-79; BIBL. 12 REF.Article

CHROMOSOME 7 SHORT-ARM INTERSTITIAL DELETION (P. 14)MOEDJONO SJ; FUNDERBURK SJ; SPARKES RS et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 44; NO 1; PP. 51-57; BIBL. 8 REF.Article

,XX,+DER(18),T(9;18)(P24;Q21) MAT: A DISTINCT PARTIAL TRISOMY 18Q- SYNDROME.BASS HN; WEBER PARISI F; SPARKES RS et al.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 5; PP. 391-395; BIBL. 9 REF.Article

EXTENDED EVALUATION OF PREVIOUSLY REPORTED TWINS WITH A RING 14 CHROMOSOME.SPARKES RS; KLISAK I; SPARKES MC et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 273-275; ABS. FR.; BIBL. 3 REF.Article

P-SYNDROME RESULTING FROM 14Q/18Q "DICENTRIC" FUSION TRANSLOCATION.FUNDERBURK SJ; SPARKES RS; KLISAK I et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 243-250; BIBL. 16 REF.Article

PHENOTYPIC VARIATION IN TWO PATIENTS WITH A RING CHROMOSOME 22FUNDERBURK SJ; SPARKES RS; KLISAK I et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 5; PP. 305-310; BIBL. 23 REF.Article