Preferential loss of the paternal alleles in the 18q- syndromeCODY, J. D; PIERCE, J. F; BRKANAC, Z et al.American journal of medical genetics. 1997, Vol 69, Num 3, pp 280-286, issn 0148-7299Article

Growth hormone deficiency associated in the 18q deletion syndromeGHIDONI, P. D; HALE, D. E; CODY, J. D et al.American journal of medical genetics. 1997, Vol 69, Num 1, pp 7-12, issn 0148-7299Article

A new deletion of 18q23 with few typical features of the 18q - syndromeKOHONEN-CORISH, M; STRATHDEE, G; OVERHAUSER, J et al.Journal of medical genetics. 1996, Vol 33, Num 3, pp 240-243, issn 0022-2593Article

An unbalanced translocation 46,XX, +der(18)t(18;21)(q12.2;q11.2)mat, -21 associated with maternal isodisomy 18pter→18q12.2DE RAVEL, Thomy J. L; MATTHIJS, Gert; FRYNS, Jean-Pierre et al.Annales de génétique (Paris). 2001, Vol 44, Num 2, pp 63-66, issn 0003-3995Article

Growth hormone insufficiency associated with haploinsufficiency at 18q23CODY, J. D; HALE, D. E; BRKANAC, Z et al.American journal of medical genetics. 1997, Vol 71, Num 4, pp 420-425, issn 0148-7299Article

Ring chromosome 18 in a fetus with only facial anomaliesLOS, F. J; VAN DEN BERG, C; BRAAT, A. P. G et al.American journal of medical genetics. 1996, Vol 66, Num 2, pp 216-220, issn 0148-7299Article

Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetusVELAGALETI, G. V. N; CARPENTER, N. J; THARAPEL, A. T et al.Annales de génétique (Paris). 1997, Vol 40, Num 3, pp 154-157, issn 0003-3995Article

Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophreniaMORS, O; EWALD, H; BLACKWOOD, D et al.British journal of psychiatry (Print). 1997, Vol 170, Num MAR, pp 278-280, issn 0007-1250Article

The phenotype of a 45,X male with a Y/18 translocationGIMELLI, G; CINTI, R; VARONE, P et al.Clinical genetics. 1996, Vol 49, Num 1, pp 37-41, issn 0009-9163Article

Chromosome 18 translocation (18;21) (p11.1;p11.1) associated with psychosis in one familySMITH, A. B; PETERSON, P; WIELAND, J et al.American journal of medical genetics. 1996, Vol 67, Num 6, pp 560-563, issn 0148-7299Article

Analysis of clinical variation seen in patients with 18q terminal deletionsSTRATHDEE, G; ZACKAI, E. H; SHAPIRO, R et al.American journal of medical genetics. 1995, Vol 59, Num 4, pp 476-483, issn 0148-7299Article

Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniquesQUMSIYEH, M. B; TOMASI, A; TASLIMI, M et al.Journal of medical genetics. 1995, Vol 32, Num 12, pp 991-993, issn 0022-2593Article

Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridizationDARNAUDE, M. T; DIAZ DE BUSTAMANTE, A; CABELLO, P et al.Annales de génétique (Paris). 1996, Vol 39, Num 2, pp 61-63, issn 0003-3995Article

Detection of chromosome 18 rearrangement in synovial sarcoma by fluorescence in situ hybridizationPOTEAT, H. T; CORSON, J. M; FLETCHER, J. A et al.Cancer genetics and cytogenetics. 1995, Vol 84, Num 1, pp 76-81, issn 0165-4608Article

High recurrence of recombinants in a family with pericentric inversion of chromosome 18MEJIA-BALTODANO, G; BOBADILLA, L; GONZALEZ, R.-M et al.Annales de génétique (Paris). 1997, Vol 40, Num 3, pp 164-168, issn 0003-3995Article

Familial deletion of chromosome 18 (p11.2)VELAGALETI, G. V. N; HARRIS, S; CARPENTER, N. J et al.Annales de génétique (Paris). 1996, Vol 39, Num 4, pp 201-204, issn 0003-3995Article

18p Monosomy with midline defects and a de novo satellite identified by FISHTAINE, L; GOIZET, C; WEN, Z. Q et al.Annales de génétique (Paris). 1997, Vol 40, Num 3, pp 158-163, issn 0003-3995Article

Translocation t(11;18)(q21;q21) in gastric B-cell lymphomasTORACCHIO, Sonia; OTA, Hiroyoshi; DE JONG, Daphne et al.Cancer science. 2009, Vol 100, Num 5, pp 881-887, issn 1347-9032, 7 p.Article

Determination of a minimal region of loss of heterozygosity on chromosome 18q21.33 in osteosarcomaJOHNSON-PAIS, Teresa L; NELLISSERY, Maggie J; AMMERMAN, Donald G et al.International journal of cancer. 2003, Vol 105, Num 2, pp 285-288, issn 0020-7136, 4 p.Article

Acute myelomonocytic leukemia with t(1;18) in an adult patientZAMECNIKOVA, Adriana; VRANOVSKY, Andrej; GYARFAS, Jan et al.Cancer genetics and cytogenetics. 2002, Vol 133, Num 2, pp 185-186, issn 0165-4608Article

Acute myeloid leukemia with t(5;18)(q35;q21)WANG, Eunice S; MASLAK, Peter; CATHCART, Kathleen et al.Cancer genetics and cytogenetics. 2001, Vol 127, Num 1, pp 71-73, issn 0165-4608Article

Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18STANKIEWICZ, Paweł; BROZEK, Izabela; MAZURCZAK, Tadeusz et al.American journal of medical genetics. 2001, Vol 101, Num 3, pp 226-239, issn 0148-7299Article

Recours au diagnostic prénatal rapide par l'analyse FISH des cellules du liquide amniotique non cultivées = Quick prenatal diagnosis by fluorescence in situ hybridization analysis of amniotic liquid uncultured cellsMARGUERAT, P; GAIDE, A.-C; THONNEY, F et al.Revue médicale de la Suisse romande. 2000, Vol 120, Num 5, pp 401-407, issn 0035-3655Article

Cryptic translocation t(5;18) in familial mental retardationVOGELS, Annick; DEVRIENDT, Koen; VERMEESCH, Joris R et al.Annales de génétique (Paris). 2000, Vol 43, Num 3-4, pp 117-123, issn 0003-3995Article

Microdissection : a precise method to disclose the parental origin of supernumerary marker chromosomesFRIEDRICH, Ursula; BUGGE, Merete; HOUMAN, Mette et al.Annales de génétique (Paris). 2000, Vol 43, Num 2, pp 109-110, issn 0003-3995Article