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Results: 17

1.

Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.

Goumy C, Bonnet-Dupeyron MN, Cherasse Y, Laurichesse H, Jaffray JY, Lacroute G, Geneix A, Lemery D, Vago P.

Prenat Diagn. 2004 Apr;24(4):249-56.

PMID:
15065097
[PubMed - indexed for MEDLINE]
2.

Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation.

Metzke-Heidemann S, Kuhling-von Kaisenberg H, Caliebe A, Janssen D, Jonat W, Grote W, von Kaisenberg CS.

Am J Med Genet A. 2004 Apr 15;126A(2):197-203.

PMID:
15057986
[PubMed - indexed for MEDLINE]
3.

Prenatal diagnosis of de novo terminal deletion of chromosome 7q.

Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Lee MS, Wang W.

Prenat Diagn. 2003 May;23(5):375-9.

PMID:
12749033
[PubMed - indexed for MEDLINE]
4.

Cytogenetic analysis of meiotic segregation in sperm from two males heterozygous for reciprocal translocations using PRINS and humster techniques.

Pellestor F, Girardet A, Coignet L, Andréo B, Lefort G, Charlieu JP.

Cytogenet Cell Genet. 1997;78(3-4):202-8.

PMID:
9465888
[PubMed - indexed for MEDLINE]
5.

Currarino triad with a terminal deletion 7q35-->qter.

Masuno M, Imaizumi K, Aida N, Tanaka Y, Sekido K, Ohhama Y, Nishi T, Kuroki Y.

J Med Genet. 1996 Oct;33(10):877-8.

PMID:
8933345
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin.

Hoo JJ, Chao M, Szego K, Rauer M, Echiverri SC, Harris C.

Am J Med Genet. 1995 Sep 25;58(4):299-304.

PMID:
8533837
[PubMed - indexed for MEDLINE]
7.

Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.

Sullivan BA, Leana-Cox J, Schwartz S.

Am J Med Genet. 1993 Aug 15;47(2):223-30.

PMID:
8213910
[PubMed - indexed for MEDLINE]
8.

Normal Hageman factor level in 7q deletion syndrome.

Kawashima H, Taniguchi N.

Clin Genet. 1981 Mar;19(3):207-8. No abstract available.

PMID:
7273466
[PubMed - indexed for MEDLINE]
9.

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]
10.

Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.

Young RS, Weaver DD, Kukolich MK, Heerema NA, Palmer CG, Kawira EL, Bender HA.

Am J Med Genet. 1984 Feb;17(2):437-50.

PMID:
6199974
[PubMed - indexed for MEDLINE]
11.

Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7.

Baeteman MA, Philip N, Mattei MG, Mattei JF.

Clin Genet. 1985 Jun;27(6):564-9.

PMID:
3839444
[PubMed - indexed for MEDLINE]
12.

The phenotype of partial dup(7q) reconsidered: a report of five new cases.

Forabosco A, Baroncini A, Dalpra L, Chessa L, Giannotti A, Maccagnani F, Dallapiccola B.

Clin Genet. 1988 Jul;34(1):48-59.

PMID:
3409538
[PubMed - indexed for MEDLINE]
13.

Partial trisomy 10p.

Grosse KP, Schwanitz G, Singer H, Wieczorek V.

Humangenetik. 1975 Sep 10;29(2):141-4.

PMID:
1176136
[PubMed - indexed for MEDLINE]
14.

[Prenatal diagnosis of chromosome abnormalities. Three years of experience].

Boue J, Boue A, Girard S, Thepot F.

Arch Fr Pediatr. 1976 Aug-Sep;33(7):653-64. French.

PMID:
999438
[PubMed - indexed for MEDLINE]
15.

Hageman (factor XII) locus on 7q?: report of a second case with del(7)q35 and normal factor XII level.

Francke U.

Hum Genet. 1978 Dec 29;45(3):363-7. No abstract available.

PMID:
738736
[PubMed - indexed for MEDLINE]
16.

Systematic analysis of 95 reciprocal translocations of autosomes.

Aurias A, Prieur M, Dutrillaux B, Lejeune J.

Hum Genet. 1978 Dec 29;45(3):259-82.

PMID:
738728
[PubMed - indexed for MEDLINE]
17.

[Monosomy 7qter (author's transl)].

Turleau C, de Grouchy J, Perignon F, Lenoir G.

Ann Genet. 1979;22(4):242-4. French.

PMID:
317790
[PubMed - indexed for MEDLINE]

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