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Items: 15

1.

Translocation (16;17)(q22;p13) is a recurrent anomaly of aneurysmal bone cysts.

Herens C, Thiry A, Dresse MF, Born J, Flagothier C, Vanstraelen G, Allington N, Bex V.

Cancer Genet Cytogenet. 2001 May;127(1):83-4.

PMID:
11408073
2.

Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.

Piram A, Ortolan D, Peres LC, Pina-Neto JM, Riegel M, Schinzel A.

Am J Med Genet A. 2003 Jul 15;120A(2):247-52. Review.

PMID:
12833408
3.

Chromosome banding analysis of gynecomastias and breast carcinomas in men.

Teixeira MR, Pandis N, Dietrich CU, Reed W, Andersen J, Qvist H, Heim S.

Genes Chromosomes Cancer. 1998 Sep;23(1):16-20. Review.

PMID:
9713992
4.

Ring chromosome 17 syndrome with monosomy 17 mosaicism: case report and literature review.

Endo A, Uesato T, Minato M, Takada M, Takahashi S, Harada K.

Acta Paediatr. 1999 Sep;88(9):1040-3. Review. No abstract available.

PMID:
10519353
5.

Chromosomes as markers in human cancer.

Sandberg AA.

Int Adv Surg Oncol. 1981;4:311-36. Review. No abstract available.

PMID:
7019095
6.

Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome.

Midro AT, Panasiuk B, Tümer Z, Stankiewicz P, Silahtaroglu A, Lupski JR, Zemanova Z, Stasiewicz-Jarocka B, Hubert E, Tarasów E, Famulski W, Zadrozna-Tołwińska B, Wasilewska E, Kirchhoff M, Kalscheuer V, Michalova K, Tommerup N.

Am J Med Genet A. 2004 Jan 15;124A(2):179-91. Review.

PMID:
14699618
7.

The karyotype in refractory anaemia and pre-leukaemia.

Sokal G, Michaux JL, van den Berghe H.

Clin Haematol. 1980 Feb;9(1):129-39. Review. No abstract available.

PMID:
6989532
8.

Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature.

Park IJ, Park JE, Kim HJ, Jung HJ, Lee WG, Cho SR.

Cancer Genet Cytogenet. 2010 Jan 1;196(1):105-8. doi: 10.1016/j.cancergencyto.2009.08.017. Review.

PMID:
19963144
9.

A new complex variant t(4;15;17) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation and literature review.

Liu S, Li Q, Pang W, Bo L, Qin S, Liu X, Teng Q, Qian L, Wang J.

Cancer Genet Cytogenet. 2001 Oct 1;130(1):33-7. Review.

PMID:
11672771
10.

Complex chromosomal rearrangements (CCR) and their genetic consequences.

Kleczkowska A, Fryns JP, Van den Berghe H.

J Genet Hum. 1982 Oct;30(3):199-214. Review. No abstract available.

PMID:
6759619
11.

[Microcytogenetics 1988. Mendelian disease entities related to microdeletions, duplications, translocations].

Turleau C, de Grouchy J.

Ann Pediatr (Paris). 1988 Dec;35(10):711-8. Review. French. No abstract available.

PMID:
3064676
12.

ABC of clinical genetics. Chromosomal disorders. I.

Kingston HM.

BMJ. 1989 Mar 11;298(6674):663-5. Review. No abstract available.

13.

[Congenital oculomotor apraxia associated with duplication of band P13 of chromosome 5. Review of the literature].

Martín Carballo G, Ramos Lizana J, García Peñas JJ, Muñoz Hiraldo ME, Vara T, de Sarría MJ, Arcas Martínez J.

An Esp Pediatr. 1993 Jan;38(1):57-60. Review. Spanish. No abstract available.

PMID:
8439082
14.

Chromosomal aberrations in musculoskeletal tumours: clinical importance.

Rydholm A.

J Bone Joint Surg Br. 1996 May;78(3):501-6. Review. No abstract available.

PMID:
8636199
15.

Chromosomes in lymphomas and solid tumors.

Heerema NA.

Cancer Invest. 1998;16(3):183-7. Review. No abstract available.

PMID:
9541633

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