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Prenatal diagnosis of the derivative chromosome 22 associated with cat eye syndrome by fluorescence in situ hybridizationREESER, S. L; DONNENFELD, A. E; MILLER, R. C et al.Prenatal diagnosis. 1994, Vol 14, Num 11, pp 1029-1034, issn 0197-3851Article

Skeletal anomalies and deformities in patients with deletions of 22q11MING, J. E; MCDONALD-MCGINN, D. M; MEGERIAN, T. E et al.American journal of medical genetics. 1997, Vol 72, Num 2, pp 210-215, issn 0148-7299Article

Long arm deletion of chromosome 22KIRSHENBAUM, G; CHMURA, M; RHONE, D. P et al.Journal of medical genetics. 1988, Vol 25, Num 11, issn 0022-2593, 780 [1 p.]Article

Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literatureLURIE, I. W; SUPOVITZ, K. R; ROSENBLUM-VOS, L. S et al.Genetic counseling. 1994, Vol 5, Num 1, pp 11-14, issn 1015-8146Conference Paper

Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequenceMASCARELLO, J. T; BASTIAN, J. F; JONES, M. C et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 112-114, issn 0148-7299, 3 p.Article

Translocation breakpoint mapping: molecular and cytogenetic studies of chromosome 22EMANUEL, B. S; NOWELL, P. C; MCKEON, C et al.Cancer genetics and cytogenetics. 1986, Vol 19, Num 1-2, pp 81-92, issn 0165-4608Article

Deletion of 22q11.2KATES, Wendy R; EMANUEL, Beverly S.Developmental disabilities research reviews. 2008, Vol 14, Num 1, 76 p.Serial Issue

Submicroscopic deletions at 22q11.2 : variability of the clinical picture and delineation of a commonly deleted regionLINDSAY, E. A; GREENBERG, F; SHAFFER, L. G et al.American journal of medical genetics. 1995, Vol 56, Num 2, pp 191-197, issn 0148-7299Article

Trisomy of chromosome 22 in acute meylomonocytic leukemiaNIEMEYER, M. M. G; HAAK, H. L; AUGUSTINUS, E et al.Cancer genetics and cytogenetics. 1986, Vol 20, Num 3-4, pp 371-374, issn 0165-4608Article

Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletionSTEWART, T. L; IRONS, M. B; COWAN, J. M et al.Teratology (Philadelphia, PA). 1999, Vol 59, Num 1, pp 20-22, issn 0040-3709Article

Juvenile rheumatoid arthritis and del(22q11) syndrome : a non-random associationVERLOES, A; CURRY, C; JAMAR, M et al.Journal of medical genetics. 1998, Vol 35, Num 11, pp 943-947, issn 0022-2593Article

Kabuki (Niikawa-Kuroki) syndrome associated with immunodeficiencyCHRZANOWSKA, K. H; KRAJEWSKA-WALASEK, M; KUS, J et al.Clinical genetics. 1998, Vol 53, Num 4, pp 308-312, issn 0009-9163Article

Another critical region for deletion of 22q11 : A study of 100 patientsKURAHASHI, H; TSUDA, E; KOHAMA, R et al.American journal of medical genetics. 1997, Vol 72, Num 2, pp 180-185, issn 0148-7299Article

Deletion of chromosome 22q11 and pseudohypoparathyroidismCRAIGEN, W. J; LINDSAY, E. A; BRICKER, J. T et al.American journal of medical genetics. 1997, Vol 72, Num 1, pp 63-65, issn 0148-7299Article

Thymoma with a t(15;22)(q11;q11)DAL CIN, P; DE WOLF-PEETERS, C; DENEFFE, G et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 181-183, issn 0165-4608Article

Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversionPRASHER, V. P; ROBERTS, E; NORMAN, A et al.Journal of medical genetics. 1995, Vol 32, Num 4, pp 306-308, issn 0022-2593Article

Velo-cardio-facial syndrome : frequency and extent of 22q11 deletionsLINDSAY, E. A; GOLDBERG, R; JURECIC, V et al.American journal of medical genetics. 1995, Vol 57, Num 3, pp 514-522, issn 0148-7299Article

Clinical, cytogenetic, and molecular characterization of severe patients with deletions of chromosome 22q13.3NESSLINGER, N. J; GORSKI, J. L; KURCZYNSKI, T. W et al.American journal of human genetics. 1994, Vol 54, Num 3, pp 464-472, issn 0002-9297Article

Microdeletions of chromosomal region 22q11 in patients with congeintal conotruncal cardiac defectsGOLDMUNTZ, E; DRISCOLL, D; BUDARF, M. L et al.Journal of medical genetics. 1993, Vol 30, Num 10, pp 807-812, issn 0022-2593Article

A recurring translocation, t(11;22)(p13;q11.2), characterizes intra-abdominal desmoplastic small round-cell tumorsRODRIGUEZ, E; SREEKANTAIAH, C; GERALD, W et al.Cancer genetics and cytogenetics. 1993, Vol 69, Num 1, pp 17-21, issn 0165-4608Article

Analysis of sperm chromosome complements from a man heterozygous for a Robertsonian translocation 45,XY,t(15q;22q)MARTIN, R. H; KO, E; HILDEBRAND, K et al.American journal of medical genetics. 1992, Vol 43, Num 5, pp 855-857, issn 0148-7299Article

No correlation between site of breakpoint in the BCR gene and platelet counts in Philadelphia chromosome-positive CMLOPALKA, B; WANDL, U. B; KLOKE, O et al.Leukemia research. 1992, Vol 16, Num 9, pp 937-939, issn 0145-2126Article

Correlation between cytogenetic data and ganglioside pattern in human meningiomasBERRA, B; PAPI, L; BIGOZZI, U et al.International journal of cancer. 1991, Vol 47, Num 3, pp 329-333, issn 0020-7136, 5 p.Article

Sir A.E. Garrod, congenital heart disease in down syndrome, and the doctrine of fetal endocarditisLUBINSKY, M. S.American journal of medical genetics. 1991, Vol 40, Num 1, pp 27-30, issn 0148-7299Article