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Rare 15q duplication in an abortusJALAL, S. M; DAY, D. W; NELSON, M. C et al.American journal of medical genetics. 1989, Vol 33, Num 3, pp 422-423, issn 0148-7299Article

Proximal 15q variant with normal phenotype in three unrelated individualsBROOKWELL, R; VELEBA, A.Clinical genetics. 1987, Vol 31, Num 5, pp 311-314, issn 0009-9163Article

Intrachromosomal triplication of 15q11-q13SCHINZEL, A. A; BRECEVIC, L; BERNASCONI, F et al.Journal of medical genetics. 1994, Vol 31, Num 10, pp 798-803, issn 0022-2593Article

A case of ring chromosome 15 accompanied by almost normal intelligenceKITATANI, M; TAKAHASHI, H; OZAKI, M et al.Human genetics. 1990, Vol 85, Num 1, pp 138-139, issn 0340-6717, 2 p.Article

Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromesWILSON, G. N; SAUDER, S. E; BUSH, M et al.Journal of medical genetics. 1985, Vol 22, Num 3, pp 233-236, issn 0022-2593Article

Interstitial deletion of chromosome 15: two casesFORMIGA, L. DE F; POENARU, L; COURONNE, F et al.Human genetics. 1988, Vol 80, Num 4, pp 401-404, issn 0340-6717Article

Säuglingshypotonie, Adipositas, Hypogenitalismus und Oligophrenie neue Gesichtspunkte zur Ätiologie und Symptomatik des Prader-Willi-Syndroms = Hypotonie musculaire du nourrisson, obésité, hypogénitalisme et arriération mentale - nouveaux aspects des données étiologiques et symptomatiques du syndrome de Prader-Willi = Muscular hypotonia in infans, obesity, hypogenitalism and mental retardation-new aspects on the etiologic features and counseling in cases of Prader-Willi syndromeWITKOWSKI, R; ULLRICH, E; PIETSCH, P et al.Psychiatrie, Neurologie und medizinische Psychologie. 1985, Vol 37, Num 5, pp 255-261, issn 0033-2739Article

Abnormalities of chromosome bands 15q13-15 in childhood acute lymphoblastic leukemiaHEEREMA, Nyla A; SATHER, Harland N; GAYNON, Paul S et al.Cancer. 2002, Vol 94, Num 4, pp 1102-1110, issn 0008-543XArticle

Complex variant 15;17 translocations in acute promyelocytic leukemia : A case report and review of three-way translocationsWAN, T. S. K; CHIM, C. S; SO, C. K et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 2, pp 139-143, issn 0165-4608Article

A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-techniqueVERMA, R. S; KLEYMAN, S. M; GIRIDHARAN, R et al.Clinical genetics. 1996, Vol 49, Num 6, pp 303-305, issn 0009-9163Article

Extreme variant of the short arm of chormosome 15FRIEDRICH, U; CAPRANI, M; NIEBUHR, E et al.Human genetics. 1996, Vol 97, Num 6, pp 710-713, issn 0340-6717Article

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infantMILUNSKY, J. M; WYANDT, H. E; XIN-LI HUANG et al.American journal of medical genetics. 1996, Vol 61, Num 3, pp 269-273, issn 0148-7299Article

Uniparental paternal disomy in Angelman's syndromeMALCOLM, S; CLAYTON-SMITH, J; NICHOLS, M et al.Lancet (British edition). 1991, Vol 337, Num 8743, pp 694-697, issn 0140-6736, 4 p.Article

Angelman syndrome : three molecular classes identified with chromosome 15q11q13-specific DNA markersKNOLL, J. H. M; NICHOLLS, R. D; MAGENIS, R. E et al.American journal of human genetics. 1990, Vol 47, Num 1, pp 149-154, issn 0002-9297, 6 p.Article

Craniosynostosis in an infant with an intestitial deletion of 15q [46,XY, del(15)(q15q22.1)]FUKUSHIMA, Y; WAKUI, K; NISHIDA, T et al.American journal of medical genetics. 1990, Vol 36, Num 2, pp 209-213, issn 0148-7299, 5 p.Article

Cytogenetic and clinical studies in acute promyelocytic leukemia (M3) and cytologic M3 variant (M3V)MONTALDI, A; DRAGONE, P; SCALA, D et al.Cancer genetics and cytogenetics. 1989, Vol 37, Num 2, pp 263-268, issn 0165-4608Article

Balanced X;15 translocation 46,X,t(X;15)(q21;q23) associated with primary amenorrheaXUE-WEN JI; XIAO-YI CHEN; JUN TAN et al.American journal of medical genetics. 1988, Vol 31, Num 4, pp 783-786, issn 0148-7299Article

Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomyGARCIA-ESQUIVEL, L; RIVERA, H; SANCHEZ-CORONA, J et al.Annales de génétique (Paris). 1987, Vol 30, Num 2, pp 94-97, issn 0003-3995Article

High resolution pattern of an inverted duplication (15)HOO, J. J.Clinical genetics. 1986, Vol 29, Num 3, pp 241-245, issn 0009-9163Article

Infertility associated with two accessory bisatellited chromosomesMARTIN-LUCAS, M. A; PEREZ-CASTILLO, A; ABRISQUETA, J. A et al.Human genetics. 1986, Vol 73, Num 2, pp 133-136, issn 0340-6717Article

Autistic symptoms among children and young adults with isodicentric chromosome 15RINEER, S; FINUCANE, B; SIMON, E. W et al.American journal of medical genetics. 1998, Vol 81, Num 5, pp 428-433, issn 0148-7299Article

Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15CHEUNG, S. W; SHAFFER, L. G; RICHARDS, C. S et al.American journal of medical genetics. 1997, Vol 72, Num 1, pp 47-50, issn 0148-7299Article

Distinct 15q genotypes in Russell-Silver and ring 15 syndromesROGAN, P. K; SEIP, J. R; DRISCOLL, D. J et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 10-15, issn 0148-7299Article

Ring chromosome 15 syndrome in an adult femaleMATSUISHI, T; YAMADA, Y; ENDO, K et al.JIDR. Journal of intellectual disability research (Print). 1996, Vol 40, Num 5, pp 478-481, issn 0964-2633Article