119 related articles for article (PubMed ID: 953216)
1. 9pter leads p22 deletion syndrome: a case report.
Allderdice PW; Heneghan WD; Felismino ET
Birth Defects Orig Artic Ser; 1976; 12(5):151-5. PubMed ID: 953216
[No Abstract] [Full Text] [Related]
2. 46, Del (9) (22:), a new deletion syndrome.
Alfi OS; Sanger RG; Sweeny AE; Donnell GN
Birth Defects Orig Artic Ser; 1974; 10(8):27-34. PubMed ID: 4458825
[No Abstract] [Full Text] [Related]
3. A patient with interstitial deletion 7 (p13 leads to p21).
Müller U; Staudt F; Hameister H
Ann Genet; 1981; 24(4):239-41. PubMed ID: 6800299
[No Abstract] [Full Text] [Related]
4. [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]
5. Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.
Tenconi R; Baccichetti C; Anglani F; Pellergrino PA; Kaplan JC; Junien C
Ann Genet; 1975 Jun; 18(2):95-8. PubMed ID: 1081371
[TBL] [Abstract][Full Text] [Related]
6. [Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].
Ayraud N; Rovinski J; Lambert JC; Galiana A
Ann Genet; 1976 Dec; 19(4):265-8. PubMed ID: 797303
[TBL] [Abstract][Full Text] [Related]
7. The 9p--syndrome.
Alfi OS; Donnell GN; Derencsenyi A
Birth Defects Orig Artic Ser; 1976; 12(5):157-60. PubMed ID: 953217
[No Abstract] [Full Text] [Related]
8. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
Lajarrige C; Bouquier JJ; Ronayette D; Tchertoff C; Faugeras C; Barthe D; Laleu J
Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
[No Abstract] [Full Text] [Related]
9. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Chromosome 11 long arm partial deletion: a new syndrome.
Engel E; Hirshberg CS; Cassidy SB; McGee BJ
Am J Ment Defic; 1976 Jan; 80(4):473-5. PubMed ID: 1247044
[TBL] [Abstract][Full Text] [Related]
12. Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.
Alfi O; Donnell GN; Crandall BF; Derencsenyi A; Menon R
Ann Genet; 1973 Mar; 16(1):17-22. PubMed ID: 4541805
[No Abstract] [Full Text] [Related]
13. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
Shapiro SD; Hansen KL; Littlefield CA
Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
[TBL] [Abstract][Full Text] [Related]
14. A case of 10p- syndrome.
Suciu S; Nanulescu M
Ann Genet; 1983; 26(2):109-11. PubMed ID: 6604484
[TBL] [Abstract][Full Text] [Related]
15. [Partial deletion of the short arm of the chromosome 9].
Serville F; Allain D; Broustet A; Martin C; Gachet M; Babin JP; Cenraud J
Ann Genet; 1976 Jun; 19(2):143. PubMed ID: 1085605
[TBL] [Abstract][Full Text] [Related]
16. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H
Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588
[TBL] [Abstract][Full Text] [Related]
17. Partial monosomy 10p syndrome.
Koenig R; Kessel E; Schoenberger W
Ann Genet; 1985; 28(3):173-6. PubMed ID: 3879152
[TBL] [Abstract][Full Text] [Related]
18. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
Doco-Fenzy M; Elchardus JF; Brami G; Digeon B; Gruson N; Adnet JJ
Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534
[TBL] [Abstract][Full Text] [Related]
19. Structural variation in human nitotic chromosomes.
Leisti J
Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
[No 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]
