Clinical consequences of deletion 1p35WENGER, S. L; STEELE, M. W; BECKER, D. J et al.Journal of medical genetics. 1988, Vol 25, Num 4, issn 0022-2593, 263Article

Trisomy 1q42→qter in a sister and brother : further delineation of the trisomy 1q42→qter syndromeVERSCHUUREN-BEMELMANS, C. C; LEEGTE, B; HODENIUS, T. M. J et al.American journal of medical genetics. 1995, Vol 58, Num 1, pp 83-86, issn 0148-7299Article

Terminal deletion of chromosome 1(q43) in a female infantGARANI, G. P; TAMISARI, L; VOLPATO, S et al.Journal of medical genetics. 1988, Vol 25, Num 3, pp 211-212, issn 0022-2593Article

A specific syndrome due to deletion of the distal long arm of chromosome 1MEINECKE, P; VOGTEL, D.American journal of medical genetics. 1987, Vol 28, Num 2, pp 371-376, issn 0148-7299Article

A new case of distal deletion of the long arm of chromosome 1MANOUVRIER-HANU, S; WALBAUM, R; GAYOT, C et al.American journal of medical genetics. 1986, Vol 25, Num 3, pp 599-600, issn 0148-7299Article

Chromosome 1p terminal deletion : report of new findings and confirmation of two characteristic phenotypesKEPPLER-NOREUIL, K. M; CARROLL, A. J; FINLEY, W. H et al.Journal of medical genetics. 1995, Vol 32, Num 8, pp 619-622, issn 0022-2593Article

Tandem duplication (1) (q1 → q22) in a male infant with multiple congenital malformationsMERTENS, F; JOHANSSON, B; FORSLUND, M et al.Clinical genetics. 1987, Vol 32, Num 1, pp 46-48, issn 0009-9163Article

Concise review: genetic consequences of ring chromosome 1 in humansPATEL, S. V; VERMA, R. S.Dysmorphology and clinical genetics. 1988, Vol 1, Num 4, pp 148-151Article

Clinical variability of partial duplication 1q: a clinical report and literature reviewROSENTHAL, J; ABELIOVICH, D; CARMI, R et al.American journal of medical genetics. 1987, Vol 27, Num 4, pp 787-792, issn 0148-7299Article

Partial deletion of chromosome 1 in a case of acute myelocytic leukemiaCOUPLAND, L. A; JAMMU, V; PIDCOCK, M. E et al.Cancer genetics and cytogenetics. 2002, Vol 139, Num 1, pp 60-62, issn 0165-4608, 3 p.Article

Differential involvement of chromosomes 1 and 4 in the formation of chromosomal aberrations in human lymphocytes after X-irradiationBOEI, J. J. W. A; VERMEULEN, S; NATARAJAN, A. T et al.International journal of radiation biology (Print). 1997, Vol 72, Num 2, pp 139-145, issn 0955-3002Article

Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1qMOGUL, M. J; BRADY, K; BROTHMAN, A. R et al.Cancer genetics and cytogenetics. 1997, Vol 95, Num 2, pp 210-212, issn 0165-4608Article

Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidineHERNANDEZ, R; FRADY, A; ZHANG, X.-Y et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 3-4, pp 196-201, issn 0301-0171Article

Clinical relevance of loss of heterozygosity of the short arm of chromosome 1 in neuroblastoma : A single-institution studySCHLEIERMACHER, G; DELATTRE, O; PETER, M et al.International journal of cancer. 1996, Vol 69, Num 2, pp 73-78, issn 0020-7136Article

Sex reversal in a child with the karyotype 46, XY, dup (1) (p22.3p32.3)WIEACKER, P; MISSBACH, D; JAKUBICZKA, S et al.Clinical genetics. 1996, Vol 49, Num 5, pp 271-273, issn 0009-9163Article

Clonal evolution of an immunoblastic type non-Hodgkin's lymphoma with der(6)t(1;6)(q11;p11) as its primary cytogenetic abnormalityGAGOS, S; IATRIDOU-KRYKOU, K; LIOSI, A et al.Cancer genetics and cytogenetics. 1995, Vol 79, Num 1, pp 59-63, issn 0165-4608Article

Translocation (1;16) identified by chromosome painting, and PRimed IN Situ-labeling (PRINS): report of two cases and review of the cytogenetic literatureHINDKJAER, J; HAMMOUDAH, S. A. F. M; HANSEN, K. B et al.Cancer genetics and cytogenetics. 1995, Vol 79, Num 1, pp 15-20, issn 0165-4608Article

Partial monosomy of chromosome 1p36.6 : characterization of the critical region and delineation of a syndromeREISH, O; BERRY, S. A; HIRSCH, B et al.American journal of medical genetics. 1995, Vol 59, Num 4, pp 467-475, issn 0148-7299Article

Molecular analysis of a human Y;1 translocation in an azoospermic maleMARASCHIO, P; TUPLER, R; DAINOTTI, E et al.Cytogenetics and cell genetics. 1994, Vol 65, Num 4, pp 256-260, issn 0301-0171Article

Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypesESTOP, A. M; BANSAL, V; LIN, A et al.American journal of medical genetics. 1994, Vol 49, Num 4, pp 410-413, issn 0148-7299Article

A single clonal abnormality of chromosome 1 found in an adenocarcinoma of the uterusDEGER, R. B; NOUMOFF, J. S; FARUQI, S. A et al.Cancer genetics and cytogenetics. 1994, Vol 78, Num 1, pp 105-107, issn 0165-4608Article

Survival of patients with t(1;7) (p11;p11). Report of two cases and review of the literaturePEDERSEN, B.Cancer genetics and cytogenetics. 1992, Vol 60, Num 1, pp 53-59, issn 0165-4608Article

Acute myelomonocytic leukemia with bone marrow eosinophilia and inv(16)(p13q22),t(1;16)(q32;q22)MOH-YING YIP; PRAVEEN SHARMA; WHITE, L et al.Cancer genetics and cytogenetics. 1991, Vol 51, Num 2, pp 235-238, issn 0165-4608Article

Heterochromatin variants in 109 ovarian cancer patients and 192 healthy subjectsKÖPF, I; STRID, K.-G; ISLAM, M. Q et al.Hereditas (Landskrona). 1990, Vol 113, Num 1, pp 7-16, issn 0018-0661, 10 p.Article

T-cell acute lymphoblastic leukemia with t(1;18)(p36;q22)KOWAL-VERN, A; MELNYK, A.Cancer genetics and cytogenetics. 1990, Vol 50, Num 1, pp 31-33, issn 0165-4608, 3 p.Article