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Results: 1 to 20 of 23

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
11.

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

Boué A, Gallano P.

Prenat Diagn. 1984 Spring;4 Spec No:45-67.

PMID:
6463033
[PubMed - indexed for MEDLINE]
12.

Pericentric inversions. Problems and significance for clinical genetics.

Kaiser P.

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

PMID:
6389316
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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.

PMID:
3585946
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

Daniel A, Hook EB, Wulf G.

Am J Med Genet. 1989 May;33(1):14-53.

PMID:
2750783
[PubMed - indexed for MEDLINE]
19.

Population studies of INV(9) chromosomes in 4,300 Japanese: incidence, sex difference and clinical significance.

Yamada K.

Jpn J Hum Genet. 1992 Dec;37(4):293-301.

PMID:
1297449
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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