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Results: 1 to 20 of 33

1.

Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations.

Chuang L, Kuo PL, Yang HB, Chien CH, Chen PY, Chang CH, Chang FM.

Prenat Diagn. 2003 Feb;23(2):134-7.

PMID:
12575020
[PubMed - indexed for MEDLINE]
2.

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint.

Tentler D, Brandberg G, Betancur C, Gillberg C, Annerén G, Orsmark C, Green ED, Carlsson B, Dahl N.

Am J Med Genet. 2001 Dec 8;105(8):729-36.

PMID:
11803521
[PubMed - indexed for MEDLINE]
3.

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C.

J Med Genet. 2001 Nov;38(11):740-4.

PMID:
11694545
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Candidate region for Coffin-Siris syndrome at 7q32-->34.

McGhee EM, Klump CJ, Bitts SM, Cotter PD, Lammer EJ.

Am J Med Genet. 2000 Jul 31;93(3):241-3.

PMID:
10925390
[PubMed - indexed for MEDLINE]
5.

Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7).

Löffler J, Utermann B, Duba HC, Mayr U, Utermann G, Erdel M.

Am J Med Genet. 2000 Apr 10;91(4):291-7.

PMID:
10766986
[PubMed - indexed for MEDLINE]
6.

Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly.

Chen CP, Liu FF, Jan SW, Lin CL, Lan CC.

Clin Genet. 1996 Nov;50(5):321-6.

PMID:
9007318
[PubMed - indexed for MEDLINE]
7.

Terminal deletion of 7q presenting in utero with a truncus arteriosus and nonimmune hydrops.

Finley BE, Seguin JH, Bennett TL, Ardinger R, Burlbaw J, Levitch L, Keifer C, Pasztor L.

Am J Med Genet. 1993 Aug 15;47(2):221-2.

PMID:
8213909
[PubMed - indexed for MEDLINE]
8.

Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).

D'Alessandro E, Ligas C, Lo Re ML, Marcanio MP, Gentile T, Del Porto G.

J Med Genet. 1994 May;31(5):413-5.

PMID:
8064823
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A constellation of dental anomalies in a chromosomal deletion syndrome (7q32): case report.

Pokala P, Acs G.

Pediatr Dent. 1994 Jul-Aug;16(4):306-9.

PMID:
7937265
[PubMed - indexed for MEDLINE]
10.

Different clinical features in monozygotic twins: a case of 7q--syndrome.

Tsukamoto H, Inui K, Taniike M, Kamiyama K, Hori M, Sumi K, Okada S.

Clin Genet. 1993 Mar;43(3):139-42.

PMID:
7684659
[PubMed - indexed for MEDLINE]
11.

Chromosome 7 in ataxia-telangiectasia.

Scheres JM, Hustinx TW, Weemaes CM.

J Pediatr. 1980 Sep;97(3):440-1. No abstract available.

PMID:
7411307
[PubMed - indexed for MEDLINE]
12.

Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)].

Schwartz S, Meekins J, Panny SR, Sun CC, Cohen MM.

Am J Med Genet. 1983 May;15(1):141-4.

PMID:
6859113
[PubMed - indexed for MEDLINE]
13.

Non-random in vitro 7;14 translocations detected in a routine cytogenetic series. 12 examples and their possible significance.

Wallace C, Bernstein R, Pinto MR.

Hum Genet. 1984;66(2-3):157-61.

PMID:
6714974
[PubMed - indexed for MEDLINE]
14.

Partial trisomy 7q in two siblings.

Klasen M, Schmid M, Hansmann I, Grimm T.

Ann Genet. 1983;26(2):100-2.

PMID:
6604481
[PubMed - indexed for MEDLINE]
15.

A 7q- son of an XYY father.

Kajii T, Murano I.

Jinrui Idengaku Zasshi. 1984 Sep;29(3):387-9. No abstract available.

PMID:
6533358
[PubMed - indexed for MEDLINE]
16.

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]
17.

Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites.

Barbi G, Steinbach P, Vogel W.

Hum Genet. 1984;68(4):290-4.

PMID:
6239815
[PubMed - indexed for MEDLINE]
18.

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]
19.

Partial trisomy 7 (q32----qter) syndrome in two children.

Couzin DA, Haites N, Watt JL, Johnston AW.

J Med Genet. 1986 Oct;23(5):461-5.

PMID:
3783625
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Cytogenetic study of 1,633 cases.

Wang SG, Ren GQ, Xue H, Shen QY, Song LL, Yuan P.

Chin Med J (Engl). 1988 Apr;101(4):231-6. No abstract available.

PMID:
3138079
[PubMed - indexed for MEDLINE]
Free Article

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