Seventh international workshop on human gene mapping, Los Angeles CA, August 21-August 26, 1983Cytogenetics and cell genetics. 1984, Vol 37, Num 1-4, pp 16-20, issn 0301-0171, 665 p.Conference Proceedings

Régions hétérochromatiques des chromosomes humains 1, 9, 16, Y et phénotypePODUGOL'NIKOVA, O. A; GRIGOR'EVA, N. M; BLYUMINA, M. G et al.Genetika. 1984, Vol 20, Num 3, pp 496-500, issn 0016-6758Article

Polymorphisme des régions hétérochromatiques des chromosomes 1, 9, 16, Y, et arriération mentale chez l'hommePODUGOL'NIKOVA, O. A; SUSHANLO, KH. M; BLYUMINA, M. G et al.Genetika. 1984, Vol 20, Num 1, pp 177-182, issn 0016-6758Article

Generation of mouse chromosome painting probes by DOP-PCR amplification of microdissected meiotic chromosomesXIAO, Y; DARROUDI, F; KUIPERS, A. G. J et al.Cytogenetics and cell genetics. 1996, Vol 75, Num 1, pp 63-66, issn 0301-0171Article

Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X)DANIEL, A; EKBLOM, L; PHILLIPS, S et al.American journal of medical genetics. 1984, Vol 18, Num 3, pp 483-491, issn 0148-7299Article

Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19FINELLI, P; ANTONACCI, R; MARZELLA, R et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 3, pp 325-330, issn 0888-7543Article

Mitomycin C-induced mosaicism in C-band regions of human chromosomes 1, 9, 16, and YSIMI, S.Human genetics. 1985, Vol 70, Num 3, pp 243-245, issn 0340-6717Article

Susceptibility genes for nicotine dependence : a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further studySTRAUB, R. E; SULLIVAN, P. F; NEALE, M. C et al.Molecular psychiatry. 1999, Vol 4, Num 2, pp 129-144, issn 1359-4184Article

Use of the primed in situ labelling (PRINS) technique for a rapid detection of chromosomes 13, 16, 18, 21, X and YPELLESTOR, F; GIRARDET, A; LEFORT, G et al.Human genetics. 1995, Vol 95, Num 1, pp 12-17, issn 0340-6717Article

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X : The human genomeBENTLEY, D. R; DELOUKAS, P; SCOTT, C. E et al.Nature (London). 2001, Vol 409, Num 6822, pp 942-943, issn 0028-0836Article

Initial genome scan of the NIMH genetics initiative bipolar pedigrees : Chromosomes 4, 7, 9, 18, 19, 20, and 21qDETERA-WADLEIGH, S. D; BADNER, J. A; MAXWELL, M. E et al.American journal of medical genetics. 1997, Vol 74, Num 3, pp 254-262, issn 0148-7299Article

Multiple polysomies in breast carcinomas : Preferential gain of chromosomes 1, 5, 6, 7, 12, 16, 17, 18, and 19ADEYINKA, A; MERTENS, F; IDVALL, I et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 2, pp 144-148, issn 0165-4608Article

VARIABILITE DES REGIONS HETEROCHROMATIQUES DES CHROMOSOMES HUMAINS 1, 9, 16 ET YPODUGOL'NIKOVA OA; SUSHANLO KH M; PARFENOVA IV et al.1980; GENETIKA; SUN; DA. 1980; VOL. 16; NO 4; PP. 720-726; H.T. 1; ABS. ENG; BIBL. 23 REF.Article

REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF CHROMOSOMES 13 TO 22FERGUSON SMITH MA; WESTERVELD A.1978; CYTOGENET. CELL GENET.; CHE; DA. 1978; VOL. 22; NO 1-6; PP. 111-123; BIBL. 6 P.Conference Paper

5-azacytidine-induced undercondensations in human chromosomesSCHMID, M; HAAF, T; GRUNERT, D et al.Human genetics. 1984, Vol 67, Num 3, pp 257-263, issn 0340-6717Article

Human thymosin-β₄/6-26 gene is part of a multigene family composed of seven members located on seven different chromosomesCLAUSS, I. M; WATHELET, M. G; SZPIRER, J et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 1, pp 174-180, issn 0888-7543, 7 p.Article

Relationship of the variability of the heterochromatic regions of chromosomes 1, 9, 16, and Y to some anthropometric characteristics in children with embryopathies of unknown etiology and in children with down syndromePODUGOLNIKOVA, O. A; GROGOJEVA, N. M; BLUMINA, M. G et al.Human genetics. 1984, Vol 68, Num 3, pp 254-257, issn 0340-6717Article

LATERAL ASYMMETRY IN HUMAN CHROMOSOMES 1, 3, 4, 15, AND 16BRITO BABAPULLE V.1981; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1981; VOL. 29; NO 4; PP. 198-202; BIBL. 16 REF.Article

LATERAL ASYMMETRY IN HUMAN CONSTITUTIVE HETEROCHROMATIN: FREQUENCY AND INHERITANCE.ANGELL RR; JACOBS PA.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 144-152; BIBL. 9 REF.Article

THE QUANTITATIVE ANALYSIS OF POLYMORPHISM ON HUMAN CHROMOSOMES 1,9,16, AND Y. IV: HETEROGENEITY OF A NORMAL POPULATIONPODUGOLNIKOVA OA; KOROSTELEV AP.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 2; PP. 163-169; BIBL. 11 REF.Article

GENETIC MAPPING: CHROMOSOMES 6-22KEATS B.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 5; PP. 730-742; BIBL. 39 REF.Article

AUTOSOMAL CHROMOSOME ABERRATIONS. A REVIEW OF THE CLINICAL SYNDROMES CAUSED BY STRUCTURAL CHROMOSOME ABERRATIONS, MOSAIC-TRISOMIES 8 AND 9, AND TRIPLOIDY.SCHINZEL A.1976; ERGEBN. INNEREN MED. KINDERHEILKDE; DTSCH.; DA. 1976; VOL. 38; PP. 37-94; BIBL. 9 P. 1/2Article

Ring (13),t(2;6) associated with familial fragile (16)VENTRUTO, V; RINALDI, A; RENDA, S et al.Journal of medical genetics. 1984, Vol 21, Num 3, issn 0022-2593, 233Article

De novo translocation heterozygote with three reciprocal translocationsWATT, J. L; COUZIN, D. A.Journal of medical genetics. 1983, Vol 20, Num 5, pp 385-388, issn 0022-2593Article

Four paralogous protein 4.1 genes map to distinct chromosomes in mouse and humanPETERS, L. L; WEIER, H.-U. G; WALENSKY, L. D et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 2, pp 348-350, issn 0888-7543Article