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Items: 10

1.
3.

Trisomy 1q24----1q41 in two sibs with an insertion in an inverted chromosome 4.

Stoll C, Roth MP, Dott B.

J Med Genet. 1984 Apr;21(2):133-5.

4.

[De novo appearance of a partial trisomy 1q in mosaic due to a 1;9 translocation].

Gagnon JA, Richer CL, Lemieux N, Gauthier-Chouinard M.

Ann Genet. 1984;27(1):33-7. French.

PMID:
6609670
5.

G-banded chromosomes of 3,415 liveborn infants.

Xia JH, Li LY, Dai HP, Xu J, Xu FM, He XX.

Chin Med J (Engl). 1984 Dec;97(12):921-7. No abstract available.

PMID:
6443290
6.

[De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child].

Turleau C, Roubin M, Chavin-Colin F, Satge M, de Grouchy J.

Ann Genet. 1974 Dec;17(4):291-4. French. No abstract available.

PMID:
4548828
8.

Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2.

Clark RD, Fenner-Gonzales M.

Am J Med Genet. 1989 Nov;34(3):422-6.

PMID:
2596530
9.

Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. List of all cytogenetic abnormalities detected.

Tomkins DJ, Vekemans MJ, Teshima IE, Cox DM, Dallaire L, Gagne R, Kalousek DK, Lin JC, Markovic VD, Ray M, et al.

Prenat Diagn. 1992 May;12(5):439-41. No abstract available.

PMID:
1523210
10.

A case of 46,XY,t(1;13) (q24;q32) with mental retardation.

Wilbur L, Curcuru-Giordano FM, Krishna SG, Kardon NB, Jenkins EC.

Hum Genet. 1977 Jun 30;37(2):239-42.

PMID:
885541

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