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Results: 8

1.

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications.

Kotzot D, Martinez MJ, Bagci G, Basaran S, Baumer A, Binkert F, Brecevic L, Castellan C, Chrzanowska K, Dutly F, Gutkowska A, Karaüzüm SB, Krajewska-Walasek M, Luleci G, Miny P, Riegel M, Schuffenhauer S, Seidel H, Schinzel A.

J Med Genet. 2000 Apr;37(4):281-6.

PMID:
10745046
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).

Wiktor A, Van Dyke DL, Weiss L.

Am J Med Genet. 1993 Jan 1;45(1):22-4.

PMID:
8418653
[PubMed - indexed for MEDLINE]
3.

De novo tandem duplication 17p11 leads to cen.

Docherty Z, Hultén MA, Honeyman MM.

J Med Genet. 1983 Apr;20(2):138-42. No abstract available.

PMID:
6842549
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Interstitial deletion of the short arm of chromosome 17.

Patil SR, Bartley JA.

Hum Genet. 1984;67(2):237-8. No abstract available.

PMID:
6745947
[PubMed - indexed for MEDLINE]
5.

Repeated pregnancy loss.

FitzSimmons J, Wapner RJ, Jackson LG.

Am J Med Genet. 1983 Sep;16(1):7-13.

PMID:
6638072
[PubMed - indexed for MEDLINE]
6.

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]
7.

Cytogenetic studies in a selected group of mentally retarded children.

Moghe M, Patel ZM, Peter JJ, Ambani LM.

Hum Genet. 1981;58(2):184-7.

PMID:
6456981
[PubMed - indexed for MEDLINE]
8.

Complete trisomy 17p a relatively new syndrome.

Martsolf JT, Larson L, Jalal SM, Wasdahl WA, Miller R, Kukolich M.

Ann Genet. 1988;31(3):172-4. Review.

PMID:
3066280
[PubMed - indexed for MEDLINE]

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