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Items: 11

1.

Partial trisomy 10q with mild phenotype caused by an unbalanced X;10 translocation.

Mononen T, Sharp A, Laakso M, Meltoranta RL, Valve-Dietz AK, Heinonen K.

J Med Genet. 2003 May;40(5):e61. No abstract available.

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Chromosome abnormalities in 447 couples undergoing intracytoplasmic sperm injection--prevalence, types, sex distribution and reproductive relevance.

Meschede D, Lemcke B, Exeler JR, De Geyter C, Behre HM, Nieschlag E, Horst J.

Hum Reprod. 1998 Mar;13(3):576-82.

PMID:
9572415
4.

Partial trisomy 10 mosaicism with cutaneous manifestations: report of a case and review of the literature.

Boon C, Markello T, Jackson-Cook C, Pandya A.

Clin Genet. 1996 Nov;50(5):417-21. Review.

PMID:
9007335
5.

Further delineation of the partial proximal trisomy 10q syndrome.

Aalfs CM, Hoovers JM, Nieste-Otter MA, Mannens MM, Hennekam RC, Leschot NJ.

J Med Genet. 1995 Dec;32(12):968-71.

6.

Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

Fewtrell MS, Tam PK, Thomson AH, Fitchett M, Currie J, Huson SM, Mulligan LM.

J Med Genet. 1994 Apr;31(4):325-7. Review.

7.

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.

PMID:
3970071
8.

Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entity.

Fryns JP, Kleczkowska A, Igodt-Ameye L, Van den Berghe H.

Clin Genet. 1987 Jul;32(1):61-5.

PMID:
3502695
10.

Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21).

Holden JJ, MacDonald EA.

Am J Med Genet. 1985 Feb;20(2):245-8.

PMID:
2579554

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