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au.\*:("HUSTINX TWJ")

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HERITABLE FRAGILE SITES AND LYMPHOCYTE CULTURE MEDIUM CONTAINING BRD USCHERES JMJC; HUSTINX TWJ.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 4; PP. 628-629; BIBL. 4 REF.Article

HABITUAL ABORTION AND TRANSLOCATION (22Q; 22Q): UNEXPECTED TRANSMISSION FROM A MOTHER TO HER PHENOTYPICALLY NORMAL DAUGHTERKIRKELS VGHJ; HUSTINX TWJ; SCHERES JMJC et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 456-461; BIBL. 23 REF.Article

NOMARSKI-OPTICAL STUDIES OF HUMAN CHROMOSOMES K-BANDED WITH BARIUM HYDROXIDESCHERES JMJC; HUSTINX TWJ; MERKX GFM et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 255-259; BIBL. 26 REF.Article

CHROMOSOME 7 IN ATAXIA-TELANGIECTASIASCHERES JMJC; HUSTINX TWJ; WEEMAES CMR et al.1980; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1980; VOL. 97; NO 3; PP. 440-441; BIBL. 4 REF.Article

PARTIAL TRISOMY OF CHROMOSOME 1 RESULTING FROM A COMPLEX MATERNAL REARRANGEMENT OF CHROMOSOMES 1, 5, AND 6HUSTINX TWJ; NABBEN FAE; SCHERES JMJC et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 4; PP. 353-358; BIBL. 4 REF.Article

A PRESUMPTIVE TETRASOMY FOR THE SHORT ARM OF CHROMOSOME 9 = TETRASOMIE PRESUMEE DU BRAS COURT DU CHROMOSOME 9RUTTEN FJ; SCHERES JMJC; HUSTINX TWJ et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 3; PP. 163-170; BIBL. 11 REF.Article

"REVERSE" DIFFERENTIAL STAINING OF SISTER CHROMATIDS.SCHERES JMJC; HUSTINX TWJ; RUTTEN FJ et al.1977; EXPER. CELL RES.; U.S.A.; DA. 1977; VOL. 109; NO 2; PP. 466-468; BIBL. 14 REF.Article

SELF-MUTILATION IN A CASE OF 49,XXXXY CHROMOSOMAL CONSTITUTIONKORTEN JJ; VANDORP A; HUSTINX TWJ et al.1975; J. MENTAL DEFIC. RES.; G.B.; DA. 1975; VOL. 19; NO 1; PP. 63-71; BIBL. 20 REF.Article

TRISOMY FOR THE SHORT ARM OF CHROMOSOME NO. 10 = TRISOMIE DU BRAS COURT DU CHROMOSOME NO10HUSTINX TWJ; TER HAAR BGA; SCHEERES JMJC et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 5; PP. 408-415; BIBL. 10REF.Article

AUTOSOMAL HETEROSOMAL MIXOPLOIDY: A REPORT ON TWO PATIENTS, A FEMALE WITH A 45,X/47, XX,+21 AND A MALE WITH A 45,X/47, XY,+21 CHROMOSOME CONSTITUTIONHUSTINX TWJ; HAAR BGA TER; SCHERES JMJC et al.1974; SEM. HOP., ANN. GENET.; FR.; DA. 1974; VOL. 17; NO 4; PP. 225-234; ABS. FR.; BIBL. 31REF.Article

HYPERSENSITIVITY TO IONIZING RADIATION, IN VITRO, IN A NEW CHROMOSOMAL BREAKAGE DISORDER, THE NIJMEGEN BREAKAGE SYNDROMETAALMAN RDFM; JASPERS NGJ; SCHERERES JMJC et al.1983; MUTATION RESEARCH; ISSN 0027-5107; NLD; DA. 1983; VOL. 112; NO 1; PP. 23-32; BIBL. 2 P.Article

A CASE OF CHRONIC MYELOID LEUKEMIA WITH A TRANSLOCATION (12;22) (P13;G11).VAN DER BLIJ PHILIPSEN M; BREED WPM; HUSTINX TWJ et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 229-231; BIBL. 13 REF.Article

X-LINKED CONGENITAL HYDROCEPHALUSRENIER WO; TER HAAR BGA; SLOOF JL et al.1982; CLIN. NEUROL. NEUROSURG.; ISSN 0303-8467; NLD; DA. 1982; VOL. 84; NO 2; PP. 113-123; BIBL. 2 P.Article

KARYOTYPE INSTABILITY WITH MULTIPLE 7/14 AND 7:7 REARRANGEMENTSHUSTINX TWJ; SCNERES JMJC; WEEMAES CMR et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 199-208; BIBL. 22 REF.Article

MONOSOMY 7 IN TWO PATIENTS WITH A MYELOPROLIFERATIVE DISORDER.BOETIUS G; HUSTINX TWJ; SMITS APT et al.1977; BRIT. J. HAEMATOL.; G.B.; DA. 1977; VOL. 37; NO 1; PP. 101-109; BIBL. 25 REF.Article

BLOOM'S SYNDROME IN TWO DUTCH FAMILIES.HUSTINX TWJ; TER HAAR BGA; SCHERES JMJC et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 2; PP. 85-96; BIBL. 21 REF.Article

TRISOMY 8 MOSAICISMHUSTINX TWJ; TER HAAR BGA; RUTTEN FJ et al.1975; MAANCHSCHR. KINDERGENEESKDE; NEDERL.; DA. 1975; VOL. 43; NO 5-6; PP. 138-150; H.T. 4; ABS. NEERL.; BIBL. 1 P. 1/2Article

2:2 AND 3:1 MEIOTIC DISJUNCTIONS IN A CARRIER OF A RECIPROCAL 10/14 TRANSLOCATION.SCHERES JMJC; HUSTINX TWJ; TER HAAR BGA et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 6; PP. 481-485; BIBL. 11 REF.Article

A CASE OF PARTIAL GP MONOSOMY WITH SOME UNUSUAL CLINICAL FEATURES.RUTTEN FJ; HUSTINX TWJ; DUNK TILLEMANS AAW et al.1978; ANN. GENET.; FR.; DA. 1978; VOL. 21; NO 1; PP. 51-55; ABS. FR.; BIBL. 19 REF.Article

TRISOMY 4P IN A FAMILY WITH A T (4;15)HUSTINX TWJ; GABREELS FJM; KIRKELS VGHJ et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 13-19; ABS. FR.; BIBL. 25REF.Article

CONNATAL PELIZAEUS-MERZBACHER DISEASE WITH CONGENITAL STRIDOR IN TWO MATERNAL COUSINSRENIER WO; GABREELS FJM; HUSTINX TWJ et al.1981; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1981; VOL. 54; NO 1; PP. 11-17; BIBL. 33 REF.Article

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