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Items: 1 to 20 of 22

1.

A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.

Courtens W, Wuyts W, Scheers S, Van Luijk R, Reyniers E, Rooms L, Ceulemans B, Kooy F, Wauters J.

Eur J Med Genet. 2006 Sep-Oct;49(5):402-13. Epub 2006 Jan 30. Review.

PMID:
16488200
2.

Ring chromosome 10 (p15q26) in a patient with unipolar affective disorder, multiple minor anomalies, and mental retardation.

Concolino D, Iembo MA, Moricca MT, Strisciuglio P, Marotta R, Rossi E, Giglio S.

Am J Med Genet A. 2003 Dec 1;123A(2):201-3. No abstract available.

PMID:
14598349
3.

Pure trisomy 10p resulting from an extra ring chromosome: characterization by methods of advanced molecular cytogenetics.

Chen Z, Meloni-Ehrig A, Palumbos JC, Guan XY, Carroll KL, Dent KM, Carey JC.

Am J Med Genet. 2001 Sep 1;102(4):379-82.

PMID:
11503167
4.

Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries.

Leana-Cox J, Levin S, Surana R, Wulfsberg E, Keene CL, Raffel LJ, Sullivan B, Schwartz S.

Am J Hum Genet. 1993 Jun;52(6):1067-73.

5.

Ring chromosome 10:46,XX,r(10)(p15 leads to q26).

Tsukino R, Tsuda N, Dezawa T, Ishii T, Koike M.

J Med Genet. 1980 Apr;17(2):148-50. No abstract available.

6.
7.

[Ring chromosome 10: 46,XX,r(10)(p15q26)].

Serville F, Briault R, Taillemite JL, Despoisse S, Cotoni P, Broustet A.

Ann Genet. 1982;25(3):168-71. French.

PMID:
6982669
8.

Ring chromosome 10 and its clinical features.

Nakai H, Adachi M, Katsushima N, Yamazaki N, Sakamoto M, Tada K.

J Med Genet. 1983 Apr;20(2):142-4.

9.

Duplication (17p) in a child with an isodicentric (17p) chromosome.

Mascarello JT, Jones MC, Hoyme HE, Freebury MM.

Am J Med Genet. 1983 Jan;14(1):67-72.

PMID:
6681937
10.

[Familial pericentric inversion of chromosome 10. 2 new cases].

Teyssier M, Moreau N.

Ann Genet. 1983;26(3):183-6. French.

PMID:
6606382
11.

Familial pericentric inversion (10) and its effect on two offspring.

Rodriguez MT, Martin MJ, Abrisqueta JA.

J Med Genet. 1984 Aug;21(4):317-9.

12.
13.

[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].

Dutrillaux B, Laurent C, Robert JM, Lejeune J.

Cytogenet Cell Genet. 1973;12(4):245-53. French. No abstract available.

PMID:
4752866
14.

Deletions of the long arm of chromosome 10.

Shapiro SD, Hansen KL, Pasztor LM, DiLiberti JH, Jorgenson RJ, Young RS, Moore CM.

Am J Med Genet. 1985 Jan;20(1):181-96.

PMID:
3970071
15.

Cytogenetic analysis of 688 couples experiencing multiple spontaneous abortions.

Castle D, Bernstein R.

Am J Med Genet. 1988 Mar;29(3):549-56.

PMID:
3376998
17.

Genetic counseling in families with inherited balanced translocations: experience with 36 families.

Wolff G, Back E, Arleth S, Rapp-Körner U.

Clin Genet. 1989 Jun;35(6):404-16.

PMID:
2736789
18.

Chromosome studies of males in an institution for the mentally handicapped.

English CJ, Davison EV, Bhate MS, Barrett L.

J Med Genet. 1989 Jun;26(6):379-81.

19.

Trisomy 18q: 46,XX,-10,+der(10) t(10;18) (p15;q12) pat: a case report.

Murthy SK, Kar B, Prabhakara K, Krishnamurthy DS.

Ann Genet. 1992;35(3):174-7. Review.

PMID:
1466569
20.

Ring 10 chromosome: 46,XX,r10(p15q26).

Sparkes RS, Ling SM, Muller H.

Hum Genet. 1978 Sep 19;43(3):341-5.

PMID:
700708

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