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kw.\*:("Cromosoma E18 anormal")

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Results 1 to 25 of 356

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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

Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotypeWOLFF, D. J; RAFFEL, L. J; FERRE, M. M et al.American journal of medical genetics. 1991, Vol 41, Num 3, pp 319-321, issn 0148-7299Article

Chromosome 18 en anneau: une observation = A ring 18 chromosome: on casePARQUET, P. J; MUERICE, J. P; SIMOENS, C et al.LARC médical. 1986, Vol 6, Num 4, pp 180-185, issn 0242-9462Article

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

Délétion du bras long du chromosome 18, hypothyroïdie primaire, anémie de Biermer et hypogammaglobulinémie de type IgM = Deletion of the long arm of chromosome 18, primary hypothyroidism pernicious anemia and IgM hypogammaglobulinemiaHENROT, B; NINANE, J; MERCENIER, C et al.Archives françaises de pédiatrie. 1989, Vol 46, Num 10, pp 729-732, issn 0003-9764, 4 p.Article

Prenatal diagnosis of mosaicism for del(18)(q12•2q21•1) and a normal cell lineWILSON, M. G; LIN, M. S.Journal of medical genetics. 1988, Vol 25, Num 9, pp 635-636, issn 0022-2593Article

Contribution to the 18q- syndrome. A patient with del(18) (q22.3qter)FELDING, I; KRISTOFFERSSON, U; SJOSTROM, H et al.Clinical genetics. 1987, Vol 31, Num 4, pp 206-210, issn 0009-9163Article

Brief clinical report: phenotype-karyotype correlations in dup (18q): report of a case and reviewRAZAVI-ENCHA, F; RAOUL, O; LESCS, M.-C et al.American journal of medical genetics. 1985, Vol 21, Num 3, pp 591-595, issn 0148-7299Article

Prenatal diagnosis of a case of 46, XY, 18 p-/46, XY, 18p+ mosaicismSTEPHEN, G. S; COUZIN, D. A; WATT, J. L et al.Prenatal diagnosis. 1989, Vol 9, Num 1, pp 57-60, issn 0197-3851Article

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

Appearance of isochromosome 18q can be associated with in vitro immortalization of human T lymphocytesKALTOFT, K; PEDERSEN, C. B; HANSEN, B. H et al.Cancer genetics and cytogenetics. 1995, Vol 81, Num 1, pp 13-16, issn 0165-4608Article

Mosaicism in three cases of 47, XY (or XX), +i(18)(p10) detected by interphase fish of buccal mucosaPFEIFFER, R. A; SCHULZE, T.Annales de génétique (Paris). 1994, Vol 37, Num 4, pp 210-214, issn 0003-3995Article

18p- syndrome and hypopituitarismARTMAN, H. G; MORRIS, C. A; DEAN STOCK, A et al.Journal of medical genetics. 1992, Vol 29, Num 9, pp 671-672, issn 0022-2593Article

Plasma cell leukemia with an unusual karyotype and prolonged survival with oral alkylating agent therapyWIERNIK, P. H; SCIORTINO, D; PAIETTA, E et al.Journal of cancer research and clinical oncology. 1987, Vol 113, Num 6, pp 576-578, issn 0171-5216Article

Translocations involving the X chromosome in solid tumors: presentation of two sarcomas with t(X; 18) (q13; p11)LIMON, J; DAL CIN, P; SANDBERG, A. A et al.Cancer genetics and cytogenetics. 1986, Vol 23, Num 1, pp 87-91, issn 0165-4608Article

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

Ringchromosom 18 bei einem Neugeborenen = Ring chromosome 18 in a newbornDÖTSCH, J; FÖRSTER, W; KÜHL, P. G et al.Monatsschrift für Kinderheilkunde. 1995, Vol 143, Num 5, pp 489-492, issn 0026-9298Article

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

Interstitial deletions are not the main mechanism leading to 18q deletionsSTRATHDEE, G; HARRISON, W; RIETHMAN, H. C et al.American journal of human genetics. 1994, Vol 54, Num 6, pp 1085-1091, issn 0002-9297Article

Antepartum diagnsosis of arthrogryoposis associated with trisomy 18KOPELMAN, J. N.Military medicine. 1993, Vol 158, Num 7, pp 498-499, issn 0026-4075Article

A balanced whole arm reciprocal translocation resulting in three different adverse pregnancy outcomesCOOPER, P. J; TOWE, C; CROLLA, J. A et al.Journal of medical genetics. 1993, Vol 30, Num 5, pp 417-418, issn 0022-2593Article

alternate, adjacent 2 and 3 : 1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrierCOTTON, C; CUMMINS, M; SMITH, A et al.Clinical genetics. 1993, Vol 44, Num 4, pp 193-195, issn 0009-9163Article

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