192 related articles for article (PubMed ID: 555637)
41. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
Butler LJ; Eades SM; France NE
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43. 9pter leads p22 deletion syndrome: a case report.
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44. [A case of a chromsome B4 long arm deletion (B4q-) (author's transl)].
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Taillemite JL; Portnoi MF; Van den Akker J; Leporrier N; Marmor D; Roux C
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Geneix A; Jaffray JY; Charbonne F; Perissel B; Malpuech G; Malet P; Roland MO
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50. [Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].
Dutrillaux B; Laurent C; Robert JM; Lejeune J
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53. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
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54. [Trisomy 9p gy t(4; 9) (q 34; q21) mat].
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55. Langer-Giedion syndrome with interstitial 8q-deletion.
Zabel BU; Baumann WA
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56. A case of ring 18 chromosome in a sibship with multiple spontaneous abortions.
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58. [A case of C-D translocation in a 9 year old boy and his mother].
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59. [Trisomy 9p : 2 further cases].
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60. Another case of 9P-syndrome.
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