Al Saadi A, Yang SS, Singla P (1977) Partial trisomy of chromosomes 22 and 16 in a microphtalmic infant. Am J Hum Genet 29:18A Google Scholar
Aurias A, Turc C, Michiels Y, Sinet PM, Graveleau D, Lejeune J (1975) Deux cas de trisomie 11q(q231→qter) par translocation t(11;22)(q23;q111) dans deux familles differentes. Ann Genet (Paris) 18:185–188 CAS Google Scholar
Ayraud N, Galiana A, Lloyd M, Deswarte M (1976) Trisomie 11q(q23.1→qter) par translocation maternelle t(11; 22)(q23.1;q11.1). Une nouvelle observation. Ann Genet (Paris) 19:65–68 CAS Google Scholar
Bader PI, Jansch M, Hoffman D, Palmer CG, Gerber H, Taylor G (1978) Trisomy 11q(q21→qter). Birth Defects 14:383–392 CASPubMed Google Scholar
Bass HN, Crandall BF, Sparkes RS (1973) Probable trisomy 22 identified by fluorescent and trypsin-Giemsa banding. Ann Genet (Paris) 16:189–192 CAS Google Scholar
Begleiter ML, Kulkarni P, Harris DJ (1976)Confirmation of trisomy 22 by trypsin-Giemsa staining. J Med Genet 13:517–520 ArticleCAS Google Scholar
Biederman BM, Lin CC, Lowry RB, Somerville R (1980) Tertiary trisomy (22q11q),47,+der(22),t(11;22). Hum Genet 53:173–177 ArticleCAS Google Scholar
Bofinger MK, Soukup SW (1977) Cat's eye syndrome. Partial trisomy 22 due to translocation in the mother. Am J Dis Child 131:893–897 ArticleCAS Google Scholar
Borgaonkar DS, McKusick VA, Farber PA (1973) An inherited small extra chromosome. A mother with 46,XX,t(17;22) (p1;q1) and a son with 47,XY,+der(22)mat. J Med Genet 10:379–384 ArticleCAS Google Scholar
Bühler EM, Méhes K, Müller H, Stalder GR (1972) Cat's eye syndrome, a partial trisomy 22. Hum Genet 15:150–162 Article Google Scholar
Curcio S (1967) Malformazione del retto e della vagina associata ad anomalia cromosomica (47,XX,?G+). Arch Ostet Ginecol 72:533–539 CASPubMed Google Scholar
Emanuel BS, Zackai EH, Aronson MM, Mellman WJ, Moorhead PS (1976) Abnormal chromosome 22 and recurrence of trisomy-22 syndrome. J Med Genet 73:501–506 Article Google Scholar
Feldman GM, Sparkes RS (1978) The problem of partial trisomy 22 reconsidered. Hum Genet 45:97–101 ArticleCAS Google Scholar
Fitzgerald PH (1976) Evidence that chromosome band 22q12 is concerned with cell proliferation in chronic myeloid leukaemia. Hum Genet 33:269–274 ArticleCAS Google Scholar
Foerster W, Fuhrmann W, Gutermuth M (1975) Partielle Trisomie 22 bei fraglichem Cat eye-Syndrom. Verh Ges Anthrop Humang. G. Fischer, Stuttgart, p 233 Google Scholar
Francke U, Weber F, Sparkes RS, Mattson PD, Mann J (1977) Duplication 11 (q21 to 23→qter) syndrome. Birth Defects 13:167–186 CASPubMed Google Scholar
Garlinger P, McGeary SA, Magenis E (1977) Partial trisomy 22: a recognizable syndrome. Clin Genet 12:9–16 ArticleCAS Google Scholar
Giraud F, Mattei JF, Mattei MG, Bernard R (1975) Trisomie partielle 11q et translocation familiale 11–22. Hum Genet 28:343–347 ArticleCAS Google Scholar
Gustavson KH, Hitrec V, Santesson B (1972) Three nonmongoloid patients of similar phenotype with an extra G-like chromosome. Clin Genet 3:135–146 ArticleCAS Google Scholar
Hall B (1963) Mongolism and other abnormalities in a family with trisomy 21–22 tendency. Acta Paediatr Scand Suppl 146:77–91 Article Google Scholar
Hollingworth F, Kim CM, Falek A (1979) Partial trisomy 11q with familial 11q;21q translocation. Mammalian Chromosome Newsl 20:19 Google Scholar
Hsu LYF, Shapiro LR, Gertner M, Lieber E, Hirschhorn K (1971) Trisomy 22: a clinical entity.J Pediatr 79:12–19 ArticleCAS Google Scholar
Ishmael J, Laurence KM (1965) A probable case of incomplete trisomy of a chromosome of the 13–15 group. J Med Genet 2:136–141 ArticleCAS Google Scholar
Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J (1973) An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Hum Hered 23:568–585 ArticleCAS Google Scholar
Jotterand-Bellomo M (1976/77) Trisomie 22. Arch Genet (Zur) 49/50:134–166 Google Scholar
Kadotani T, Katano T, Yamaoka H, Murakami M, Nakamoto Y, Watanabe Y(1978a) Clinical and cytogenetic features of a case with trisomy 22. Proc Jpn Acad 54:Ser B, 163–166 Article Google Scholar
Kadotani T, Katano T, Yamaoka H, Murakami M, Nakamoto Y, Watanabe Y (1979b) A case of partial trisomy 22 without cat-eye stigmata. Proc Jpn Acad 54: Ser B, 217–221 Article Google Scholar
Kessel E, Pfeiffer RA (1977) 47,XY,+der(11;22)(q23;q12)following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22. Hum Genet 37:111–116 ArticleCAS Google Scholar
Laurent C, Biemont MC, Bethenod M, Cret L, David M (1975) Deux observations de trisomie 11q(q23.1→qter) avec la même anomalie des organes génitaux externes. Ann Genet (Paris) 18:179–184 CAS Google Scholar
Lindsten J, Therkelsen AJ,Friedrich U, Jonasson J, Steenstrup OR, Wiquist N (1974) Prenatal cytogenetic diagnosis. Int J Gynaecol Obstet 12:101–111 Article Google Scholar
Lozzio CB (1969) Nonmongoloid trisomy G. Birth Defects 5:64–66 Google Scholar
Macintyre MN, Hempel JM, Walden DB, Miller RC, Greene AE, Coriell LL (1975) A (17;22) translocation, balanced, 46 chromosomes. Repository identification No.GM-119. Cytogenet Cell Genet 14:80–81 ArticleCAS Google Scholar
Macintyre MN, Walden DB, Hempel JM (1971) Tertiary trisomy in a human kindred containing a E/G translocation. Am J Hum Genet 23:431–441 CASPubMedPubMed Central Google Scholar
Malpuech G, Menut G, Raynaud EJ, Lavignon A (1970) Trisomie libre concernant un petit acrocentrique chez un sujet féminin non mongolien. trisomie 22 ou trisomie partielle. Pédiatrie 8:901–910 Google Scholar
Moore MK, Engel E (1968) G chromosome trisomy: five cases with syndromes other than classical Down's. Southern Med J 61:146–154 ArticleCAS Google Scholar
Nakai H, Yamamoto Y, Kuroki Y (1979) Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11) inherited in three generations. Hum Genet 51:349–355 ArticleCAS Google Scholar
Narahara K, Kodama Y, Kimura S, Kamoi M, Inoue H, Kimoto H (1979) A case of partial trisomy 22 resulting from maternal 11/22 translocation. Jpn J Hum Genet 24:253–258 ArticleCAS Google Scholar
Niermeijer MF, Sachs ES, Jahodava M, Tichelaar-Klepper C, Kleijer WJ, Galjaard H (1976) Prenatal diagnosis of genetic disorders. J Med Genet 13:182–194 ArticleCAS Google Scholar
Noel B, Levy M, Rethoré MO (1976) Trisomie partielle du bras long du chromosome 11 par malségrégation d'une translocation maternelle t(11;22)(q231;q111). Ann Genet (Paris) 19:137–139 CAS Google Scholar
Pai GS, Thomas GH, Leonard CO, Ward JC, Valle DL, Pyeritz RE (1979) Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of chromosome 13, and trisomy 8. John Hopkins Med J 145:162–169 CAS Google Scholar
Parslow M, Hoo JJ, Garry M, Rose F (1980) A deleted extra chromosome 22 identified by DNA replication banding. Hum Genet 53:323–326 ArticleCAS Google Scholar
Penchaszadeh VB, Coco R (1975) Trisomy 22. Two new cases and delineation of the phenotype. J Med Genet 12:193–199 ArticleCAS Google Scholar
Punnett HH, Kistenmacher ML, Toro-Sola MA, Kohn G (1973) Quinacrine fluorescence and Giemsa banding in trisomy 22. Theor Appl Genet 43:134–138 ArticleCAS Google Scholar
Ridler MA, McKeown JA (1979) 11q aneuploidy: partial monosomy and trisomy in the children of a mother with a (3;11)(p27;q23) translocation. Hum Genet 52:101–106 ArticleCAS Google Scholar
Schinzel A (1981a) Incomplete trisomy 22. II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13). Hum Genet 56:263–268 ArticleCAS Google Scholar
Schinzel A (1981b) Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22. Hum Genet 56:269–273 ArticleCAS Google Scholar
Schinzel A, Schmid W, Fraccaro M, Tiepolo L, Zuffardi O, Opitz JM, Lindsten J, Zeterqvist P, Enell H, Bacichetti C, Tenconi R, Pagon RA (1981) The “Cat eye syndrome”: Dicentric small marker chromosome probably derived from a No.22 (tetrasomy 22pter→q11) associated with a characteristic phenotype. Report of 11 cases and delineation of the clinical picture. Hum Genet (in press)
Shanske A, Acs H, Kazi R (1979) Secondary meiotic nondisjunction in a carrier of a reciprocal translocation (11;22). Am J Hum Genet 31:110A Google Scholar
Zellweger H, Ionasescu V, Simpson J, Burmeister L (1976) The problem of trisomy 22. A case report and a discussion of the variant forms. Clin Pediat 15:601–618 ArticleCAS Google Scholar
Zellweger H, Mikamo K, Abbo G (1962) Two cases of multiple malformations with an autosomal chromosomal aberration. partial trisomy D? Helv Paediatr Acta 17:290–300 CASPubMed Google Scholar
Zergollern L, Hitrec V (1979) Partial trisomy 22. Acta Med Iugosl 33:459–470 CASPubMed Google Scholar