382 related articles for article (PubMed ID: 7205434)
21. Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
Trautmann U; Pfeiffer RA; Seufert-Satomi U; Tietze HU
J Med Genet; 1993 Apr; 30(4):330-1. PubMed ID: 8487285
[TBL] [Abstract][Full Text] [Related]
22. Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).
Vermeesch JR; Fryns JP
Am J Med Genet A; 2003 Jul; 120A(2):299-300. PubMed ID: 12833421
[No Abstract] [Full Text] [Related]
23. Chromosome 7 short arm deletion, 7p21----pter.
Schömig-Spingler M; Schmid M; Brosi W; Grimm T
Hum Genet; 1986 Nov; 74(3):323-5. PubMed ID: 3781561
[TBL] [Abstract][Full Text] [Related]
24. On the deletion 4p16 Wolf-Hirschhorn syndrome.
Rivas F; Hernandez A; Nazara Z; Fragoso R; Olivares N; Rolon A; Cantu JM
Ann Genet; 1979; 22(4):228-31. PubMed ID: 317787
[TBL] [Abstract][Full Text] [Related]
25. [Wolf syndrome. Apropos of 2 cases].
García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
[TBL] [Abstract][Full Text] [Related]
26. Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.
Hamers AJ; van Kempen C
J Med Genet; 1977 Dec; 14(6):451-5. PubMed ID: 604497
[TBL] [Abstract][Full Text] [Related]
27. Determination of the breakpoints and the parental origin of a ring 22 chromosome: an analysis by high-resolution banding technique, quinacrine and silver stainings.
Naritomi K; Hirayama K
Jinrui Idengaku Zasshi; 1988 Mar; 33(1):67-73. PubMed ID: 2455825
[No Abstract] [Full Text] [Related]
28. Analysis of banding patterns in a case of ring chromosome 21.
Richer CL; Fitch N; Sitahal S; Murer-Orlando M; Jean P
Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027
[No Abstract] [Full Text] [Related]
29. 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]
30. Interstitial deletion of the long arm of chromosome 8 without Langer-Giedion syndrome.
Kazukawa S; Endo M; Fujii T; Hori A; Yamada K; Yamaguchi T; Aizawa T; Maruyama S
Jpn J Psychiatry Neurol; 1986 Jun; 40(2):221-6. PubMed ID: 3784158
[TBL] [Abstract][Full Text] [Related]
31. A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)].
Kempen C
J Med Genet; 1975 Jun; 12(2):204-7. PubMed ID: 49428
[TBL] [Abstract][Full Text] [Related]
32. MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplication.
Fryns JP; Borghgraef M; Lemmens F; van den Berghe H
Clin Genet; 1993 Sep; 44(3):146-8. PubMed ID: 8275573
[TBL] [Abstract][Full Text] [Related]
33. Interstitial deletion of chromosome 13: prognosis and adult phenotype.
Dean JC; Simpson S; Couzin DA; Stephen GS
J Med Genet; 1991 Aug; 28(8):533-5. PubMed ID: 1920369
[TBL] [Abstract][Full Text] [Related]
34. Fragile site long arm chromosome 16.
Sørensen K; Nielsen J; Holm V; Haahr J
Hum Genet; 1979 Apr; 48(1):131-4. PubMed ID: 457128
[TBL] [Abstract][Full Text] [Related]
35. Two cases of interstitial deletion 1p.
Lai MM; Robards MF; Berry AC; Fear CN; Hart C
J Med Genet; 1991 Feb; 28(2):128-30. PubMed ID: 2002484
[TBL] [Abstract][Full Text] [Related]
36. Interstitial deletion (6)q13q15.
Gershoni-Baruch R; Mandel H; Bar El H; Bar-Nizan N; Borochowitz Z; Dar H
Am J Med Genet; 1996 Apr; 62(4):345-7. PubMed ID: 8723062
[TBL] [Abstract][Full Text] [Related]
37. Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.
Silengo MC; Luzzatti L; Centerwall WR; Costello JM; Parslow M
Clin Genet; 1981 Mar; 19(3):174-80. PubMed ID: 7273460
[TBL] [Abstract][Full Text] [Related]
38. Rieger syndrome and interstitial 4q26 deletion.
Fryns JP; Van Den Berghe H
Genet Couns; 1992; 3(3):153-4. PubMed ID: 1388934
[No Abstract] [Full Text] [Related]
39. [A new clinico-cytogenetic syndrome--a proximal deletion of the short arm of chromosome 17].
Zaletaev DV; Marincheva GS
Pediatriia; 1988; (11):82-4. PubMed ID: 3226810
[No Abstract] [Full Text] [Related]
40. De novo interstitial deletion del(1)(p21p32).
Bene M; Duca-Marinescu A; Ioan D; Maximilian C
J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
