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Results: 1 to 20 of 23

PubMed Links for Books (Select 2983398)

1.

Constitutional pericentric inversion of chromosome 9 and acute leukemia.

Keung YK, Knovich MA, Powell BL, Buss DH, Pettenati M.

Cancer Genet Cytogenet. 2003 Aug;145(1):82-5.

PMID:
12885469
2.

Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant.

Lukusa T, Devriendt K, Holvoet M, Fryns JP.

Am J Med Genet. 2000 Mar 20;91(3):192-7.

PMID:
10756341
3.

Ebstein's anomaly associated with trisomy 9p.

Nakagawa M, Kato H, Aotani H, Kondo M.

Clin Genet. 1999 May;55(5):383-5. No abstract available.

PMID:
10422813
4.

Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two cases.

Cotter PD, Babu A, McCurdy LD, Caggana M, Willner JP, Desnick RJ.

Ann Genet. 1997;40(4):222-6.

PMID:
9526617
5.

Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nuclei.

Colls P, Blanco J, Martínez-Pasarell O, Vidal F, Egozcue J, Márquez C, Guitart M, Templado C.

Hum Genet. 1997 Jun;99(6):761-5.

PMID:
9187669
6.

Schizophrenia with pericentric inversion of chromosome 9: a case report.

Nanko S.

Jpn J Psychiatry Neurol. 1993 Mar;47(1):47-9.

PMID:
8411789
7.

Chromosome heteromorphisms and early recurrent abortions.

Del Porto G, D'Alessandro E, Grammatico P, Coghi IM, DeSanctis S, Giambenedetti M, Vaccarella C, Fabi R, Marcaino MF, Nicotra M.

Hum Reprod. 1993 May;8(5):755-8.

PMID:
8314973
8.

Pericentric inversion in homologues of chromosome 9.

Sudha T, Jayam S.

Jpn J Hum Genet. 1993 Sep;38(3):341-3. No abstract available.

PMID:
8260725
9.

Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations.

Cohen O, Cans C, Mermet MA, Demongeot J, Jalbert P.

Hum Genet. 1994 Feb;93(2):188-94. Review.

PMID:
8112744
10.

Duplication of the short arm of chromosome 9. Analysis of five cases.

Cuoco C, Gimelli G, Pasquali F, Poloni L, Zuffardi O, Alicata P, Battaglino G, Bernardi F, Cerone R, Cotellessa M, Ghidoni A, Motta S.

Hum Genet. 1982;61(1):3-7.

PMID:
7129421
11.
12.

Pericentric inversions. Problems and significance for clinical genetics.

Kaiser P.

Hum Genet. 1984;68(1):1-47. Review.

PMID:
6389316
13.

Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.

Varley JM, Gosden J, Hultén M.

Hum Genet. 1981;59(4):422-8. No abstract available.

PMID:
6174409
14.

A cytogenetic survey of 11,680 newborn infants.

Jacobs PA, Melville M, Ratcliffe S, Keay AJ, Syme J.

Ann Hum Genet. 1974 May;37(4):359-76. No abstract available.

PMID:
4277977
15.

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Rethoré MO, Hoehn H, Rott HD, Couturier J, Dutrillaux B, Lejeune J.

Humangenetik. 1973 Apr 16;18(2):129-38. French. No abstract available.

PMID:
4124236
16.

Unusual chromosome 9 polymorphism and reproductive failure.

Fryns JP, Kleczkowska A, Londers L, van den Berghe H.

Ann Genet. 1985;28(1):49-51.

PMID:
3874589
17.

Duplication 9p due to unequal sister chromatid exchange.

Mattina T, Sorge G, Milone G, Garozzo R, Conti L.

J Med Genet. 1987 May;24(5):303-5.

19.
20.

Trisomy 9p in a patient with a de novo 9/15 translocation.

Jacobsen P, Hobolth N, Mikkelsen M.

Clin Genet. 1975 Apr;7(4):317-24.

PMID:
1126053
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