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Items: 17

1.

Prevention strategies for age related cataract: present limitations and future possibilities.

Congdon NG.

Br J Ophthalmol. 2001 May;85(5):516-20. Review. No abstract available.

2.

Random-breakage mapping method applied to human DNA sequences.

Löbrich M, Rydberg B, Cooper PK.

Nucleic Acids Res. 1996 May 15;24(10):1802-8.

3.

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Bonné-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA.

Am J Hum Genet. 1996 Jun;58(6):1254-9.

4.

A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance.

Coon H, Jensen S, Hoff M, Holik J, Plaetke R, Reimherr F, Wender P, Leppert M, Byerley W.

Am J Hum Genet. 1993 Jun;52(6):1234-49.

5.

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

Antonarakis SE, Blouin JL, Maher J, Avramopoulos D, Thomas G, Talbot CC Jr.

Am J Hum Genet. 1993 Jun;52(6):1145-52.

6.

Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.

King A, Houlden H, Hardy J, Lane R, Chancellor A, de Belleroche J.

J Med Genet. 1993 Apr;30(4):318.

7.

Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.

Howard CM, Davies GE, Farrer MJ, Cullen LM, Coleman MM, Williamson R, Wyse RK, Palmer R, Kessling AM.

Am J Hum Genet. 1993 Aug;53(2):462-71.

8.

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.

Chettouh Z, Croquette MF, Delobel B, Gilgenkrants S, Leonard C, Maunoury C, Prieur M, Rethoré MO, Sinet PM, Chery M, et al.

Am J Hum Genet. 1995 Jul;57(1):62-71.

9.

Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.

Petersen MB, Adelsberger PA, Schinzel AA, Binkert F, Hinkel GK, Antonarakis SE.

Am J Hum Genet. 1991 Sep;49(3):529-36.

10.

Protocols to establish genotype-phenotype correlations in Down syndrome.

Epstein CJ, Korenberg JR, Annerén G, Antonarakis SE, Aymé S, Courchesne E, Epstein LB, Fowler A, Groner Y, Huret JL, et al.

Am J Hum Genet. 1991 Jul;49(1):207-35. No abstract available.

11.

A contiguous Not I restriction map of band q22.3 of human chromosome 21.

Wang D, Fang H, Cantor CR, Smith CL.

Proc Natl Acad Sci U S A. 1992 Apr 15;89(8):3222-6.

12.

No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

Pangalos C, Théophile D, Sinet PM, Marks A, Stamboulieh-Abazis D, Chettouh Z, Prieur M, Verellen C, Rethoré MO, Lejeune J, et al.

Am J Hum Genet. 1992 Dec;51(6):1240-50.

13.

DNA polymorphism analysis in families with recurrence of free trisomy 21.

Pangalos CG, Talbot CC Jr, Lewis JG, Adelsberger PA, Petersen MB, Serre JL, Rethoré MO, de Blois MC, Parent P, Schinzel AA, et al.

Am J Hum Genet. 1992 Nov;51(5):1015-27.

14.

Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

Peterson MB, Frantzen M, Antonarakis SE, Warren AC, Van Broeckhoven C, Chakravarti A, Cox TK, Lund C, Olsen B, Poulsen H, et al.

Am J Hum Genet. 1992 Sep;51(3):516-25. Erratum in: Am J Hum Genet 1993 Mar;52(3):654.

15.

A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age.

Tanzi RE, Watkins PC, Stewart GD, Wexler NS, Gusella JF, Haines JL.

Am J Hum Genet. 1992 Mar;50(3):551-8.

16.

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.

Antonarakis SE, Petersen MB, McInnis MG, Adelsberger PA, Schinzel AA, Binkert F, Pangalos C, Raoul O, Slaugenhaupt SA, Hafez M, et al.

Am J Hum Genet. 1992 Mar;50(3):544-50.

17.

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.

McGinniss MJ, Kazazian HH Jr, Stetten G, Petersen MB, Boman H, Engel E, Greenberg F, Hertz JM, Johnson A, Laca Z, et al.

Am J Hum Genet. 1992 Jan;50(1):15-28.

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