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2. Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)]. Schwartz S; Meekins J; Panny SR; Sun CC; Cohen MM Am J Med Genet; 1983 May; 15(1):141-4. PubMed ID: 6859113 [TBL] [Abstract][Full Text] [Related]
3. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25. Taysi K; Sekhon GS; Hillman RE Am J Med Genet; 1982 Dec; 13(4):423-30. PubMed ID: 7158642 [No Abstract] [Full Text] [Related]
4. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:). Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193 [No Abstract] [Full Text] [Related]
5. [Interstitial deletion of the long arm of one 11 chromosome]. Taillemite JL; Morlier BG; Roux C Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039 [TBL] [Abstract][Full Text] [Related]
6. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]. Wilson MG; Towner JW; Forsman I; Siris E Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629 [TBL] [Abstract][Full Text] [Related]
7. Deletion of 11q: report of two cases and a review. Larson SA; Yeatman GW; Riccardi VM Birth Defects Orig Artic Ser; 1976; 12(5):125-30. PubMed ID: 953212 [TBL] [Abstract][Full Text] [Related]
8. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32). Martin-Pont B; Pilczer C; Dandine M; Tamboise A Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441 [TBL] [Abstract][Full Text] [Related]
9. Interstitial deletion of long arm of chromosome 13. Carnevale A; Frias S; Alcantar R Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673 [TBL] [Abstract][Full Text] [Related]
10. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit. Fryns JP; Kleczkowska A; Decock P; Massa G; van den Berghe H Ann Genet; 1992; 35(4):234-6. PubMed ID: 1296522 [TBL] [Abstract][Full Text] [Related]
11. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3). Copelli S; del Rey G; Heinrich J; Coco R Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102 [TBL] [Abstract][Full Text] [Related]
12. The 18p- syndrome. Report of five cases. Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777 [TBL] [Abstract][Full Text] [Related]
13. Langer-Giedion syndrome with interstitial 8q-deletion. Zabel BU; Baumann WA Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298 [TBL] [Abstract][Full Text] [Related]
15. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant. Gillar PJ; Kaye CI; Ryan SG; Moore CM Am J Med Genet; 1992 Sep; 44(2):138-41. PubMed ID: 1456281 [TBL] [Abstract][Full Text] [Related]
16. Partial trisomy 7q in two siblings. Klasen M; Schmid M; Hansmann I; Grimm T Ann Genet; 1983; 26(2):100-2. PubMed ID: 6604481 [TBL] [Abstract][Full Text] [Related]
17. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8. Pai GS; Thomas GH; Leonard CO; Ward JC; Valle DL; Pyeritz RE Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337 [No Abstract] [Full Text] [Related]
18. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature. Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660 [TBL] [Abstract][Full Text] [Related]
19. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies. Back E; Hertel C; Vogel W; Bettecken F; Thiesen M Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761 [TBL] [Abstract][Full Text] [Related]
20. A clinical syndrome associated with 5p duplication and 9p deletion. Liberfarb RM; Atkins L; Holmes LB Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]