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Results: 15

1.

Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.

Tsien F, Morava E, Talarski A, Marble M.

Clin Dysmorphol. 2005 Oct;14(4):177-81.

PMID:
16155418
[PubMed - indexed for MEDLINE]
2.

Dominant inheritance of cleft palate, microstomia and micrognathia--possible linkage to the fragile site at 16q22 (FRA16B).

McKenzie F, Turner A, Withers S, Dalzell P, McGlynn M, Kirk EP.

Clin Dysmorphol. 2002 Oct;11(4):237-41.

PMID:
12401987
[PubMed - indexed for MEDLINE]
3.

Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation.

Kerbeshian J, Severud R, Burd L, Larson L.

Am J Med Genet. 2000 Feb 7;96(1):69-73.

PMID:
10686555
[PubMed - indexed for MEDLINE]
4.

Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis.

Houlston RS, Renshaw RM, James RS, Ironton R, Temple IK.

J Med Genet. 1994 Nov;31(11):884-7.

PMID:
7853376
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Chromosomal disorder and neoplastic diseases in a family with inherited fragile 16. Causality or casualty?

Ferro MT, García-Sagredo JM, Resino M, del Potro E, Villegas A, Mediavilla J, Espinós D, San Román C.

Cancer Genet Cytogenet. 1994 Dec;78(2):160-4.

PMID:
7828147
[PubMed - indexed for MEDLINE]
6.

The fragile site at 16q22, distamycin A, and the normal pachytene structure of chromosome 16: some possible interrelationships.

Hungerford DA.

Cytogenet Cell Genet. 1981;30(1):63-4.

PMID:
7261684
[PubMed - indexed for MEDLINE]
7.

Behavior of chromosome cores at heritable fragile sites: 16q22 and Xq27.

Howard-Peebles PN, Howell WM.

Cytogenet Cell Genet. 1981;31(2):115-9. No abstract available.

PMID:
7198024
[PubMed - indexed for MEDLINE]
8.

BrdU-sensitive fragile site on long arm of chromosome 16.

Croci G.

Am J Hum Genet. 1983 May;35(3):530-3. No abstract available.

PMID:
6859046
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Enhancement of a fra(16)(q22) with distamycin A: a family ascertained through an abnormal proposita.

Dunner JA, Martin AO, Traisman ES, Traisman HS, Elias S.

Am J Med Genet. 1983 Oct;16(2):277-84.

PMID:
6359880
[PubMed - indexed for MEDLINE]
10.

Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12.

Sutherland GR, Jacky PB, Baker EG.

Am J Hum Genet. 1984 Jan;36(1):110-22.

PMID:
6198907
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Cytogenetic analyses on patients with Crouzon's and Apert's syndromes.

Mark J, Lilja J, Stenman G, Lauritzen C.

Hereditas. 1986;105(1):157-9. No abstract available.

PMID:
3793513
[PubMed - indexed for MEDLINE]
12.

Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL.

Simmers RN, Sutherland GR, West A, Richards RI.

Science. 1987 Apr 3;236(4797):92-4.

PMID:
3470945
[PubMed - indexed for MEDLINE]
13.

Different inducibility and possible significance of several concomitant "fragile sites" in two brothers.

Shabtai F, Orlin J, Hart J, Halbrecht I, Klar D, Friedman J.

Hum Genet. 1986 Sep;74(1):85-9.

PMID:
3019870
[PubMed - indexed for MEDLINE]
14.

Chromosome rearrangements among couples with pregnancy losses and other adverse reproductive outcomes.

Gadow EC, Lippold S, Otano L, Serafin E, Scarpati R, Matayoshi T.

Am J Med Genet. 1991 Dec 1;41(3):279-81.

PMID:
1789279
[PubMed - indexed for MEDLINE]
15.

The outcome of pregnancy and prenatal chromosomal diagnosis of fetuses in couples including a translocation carrier.

Uehara S, Takabayashi T, Okamura K, Yajima A.

Prenat Diagn. 1992 Dec;12(12):1009-18.

PMID:
1287636
[PubMed - indexed for MEDLINE]

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