126 related articles for article (PubMed ID: 293234)
21. Parental origin of a ring 13 chromosome in a female with multiple anomalies.
Magenis RE; Wyandt HE; Overton KM; Macfarlane J
Hum Genet; 1976 Jul; 33(2):181-6. PubMed ID: 939570
[TBL] [Abstract][Full Text] [Related]
22. Familial translocation t(9;16).
Dowman C; Lockwood D; Allanson J
J Med Genet; 1989 Aug; 26(8):525-8. PubMed ID: 2671373
[TBL] [Abstract][Full Text] [Related]
23. Interstitial deletion of the long arm of chromosome 6 [del(6) (q16q22)]: case report and review of the literature.
Schwartz MF; Kaffe S; Wallace S; Desnick RJ
Clin Genet; 1984 Dec; 26(6):574-8. PubMed ID: 6499269
[TBL] [Abstract][Full Text] [Related]
24. Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46, XY or XX, del (8) (q23.3q24.13).
Fukushima Y; Kuroki Y; Izawa T
Hum Genet; 1983; 64(1):90-3. PubMed ID: 6336324
[TBL] [Abstract][Full Text] [Related]
25. An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region.
Cremers FP; Pfeiffer RA; van de Pol TJ; Hofker MH; Kruse TA; Wieringa B; Ropers HH
Hum Genet; 1987 Sep; 77(1):23-7. PubMed ID: 3476455
[TBL] [Abstract][Full Text] [Related]
26. 13q-/r(13) mosaicism.
Niikawa N; Tamura T; Tomiyasu F; Kajii T
J Med Genet; 1980 Aug; 17(4):316-9. PubMed ID: 7205909
[TBL] [Abstract][Full Text] [Related]
27. Late replication studies in a human X/13 translocation: correlation with autosomal gene expression.
Mohandas T; Crandall BF; Sparkes RS; Passage MB; Sparkes MC
Cytogenet Cell Genet; 1981; 29(4):215-20. PubMed ID: 7195326
[TBL] [Abstract][Full Text] [Related]
28. Familial t(4;13) with abnormal offspring in three generations.
Najafzadeh TM; Littman VA; Dumars KW
Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065
[TBL] [Abstract][Full Text] [Related]
29. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
de Michelena MI; Villacorta J; Chávez J
Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
[TBL] [Abstract][Full Text] [Related]
30. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.
Bernstein R; Dawson B; Kohl R; Jenkins T
J Med Genet; 1979 Aug; 16(4):254-62. PubMed ID: 290816
[TBL] [Abstract][Full Text] [Related]
31. Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11).
Mutchinick O; Ruz L; Jiménez R
Hum Genet; 1978 Nov; 45(1):89-95. PubMed ID: 730186
[TBL] [Abstract][Full Text] [Related]
32. A pericentric inversion of chromosome 9 and a rearrangement involving chromosomes 9 and 10, observed in two generations. Clinical description of chromosome 9 (p12-p21) deletion syndrome.
Fällström SP; Wahlström J
Clin Genet; 1979 Jun; 15(6):480-6. PubMed ID: 466847
[TBL] [Abstract][Full Text] [Related]
33. Deletion of band 13q21 is compatible with normal phenotype.
Couturier J; Morichon-Delvallez N; Dutrillaux B
Hum Genet; 1985; 70(1):87-91. PubMed ID: 3997156
[TBL] [Abstract][Full Text] [Related]
34. Deletions of the long arm of chromosome 10.
Shapiro SD; Hansen KL; Pasztor LM; DiLiberti JH; Jorgenson RJ; Young RS; Moore CM
Am J Med Genet; 1985 Jan; 20(1):181-96. PubMed ID: 3970071
[TBL] [Abstract][Full Text] [Related]
35. Two cases with different deletions of the long arm of chromosome 7.
Klep-de Pater JM; Bijlsma JB; Bleeker-Wagemakers EM; de France HF; de Vries-Ekkers CM
J Med Genet; 1979 Apr; 16(2):151-4. PubMed ID: 458833
[TBL] [Abstract][Full Text] [Related]
36. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
Spikes AS; Hegmann K; Smith JL; Shaffer LG
Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
[TBL] [Abstract][Full Text] [Related]
37. A new interstitial deletion of chromosome No. 4 del(4) (q22::q25).
Butler LJ; Palmer AV; Spencer T; Tabios-Broadway R; Wall WJ
Clin Genet; 1987 Apr; 31(4):199-205. PubMed ID: 3474090
[TBL] [Abstract][Full Text] [Related]
38. Chromosome 13q deletion syndrome involving 13q31‑qter: A case report.
Wang YP; Wang DJ; Niu ZB; Cui WT
Mol Med Rep; 2017 Jun; 15(6):3658-3664. PubMed ID: 28393221
[TBL] [Abstract][Full Text] [Related]
39. Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
de Pablo CE; García Sagredo JM; Ferro MT; Ferrando P; San Román C
J Med Genet; 1980 Dec; 17(6):483-6. PubMed ID: 6937620
[TBL] [Abstract][Full Text] [Related]
40. Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation.
Mattei MG; Mattei JF; Bernard R; Giraud F
Hum Genet; 1979 Sep; 51(1):55-61. PubMed ID: 500092
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]