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Items: 1 to 20 of 262

1.

Deletion of the distal long arm of chromosome 1: a definable syndrome.

Johnson VP, Heck LJ, Carter GA, Flom JO.

Am J Med Genet. 1985 Dec;22(4):685-94.

PMID:
4073121
2.

A chromosome 1q44 deletion in a 4-month-old girl; The first report in Korea.

Cho JH, Song ES, Kim HN, Oh BS, Choi YY.

Korean J Pediatr. 2014 Jun;57(6):292-6. doi: 10.3345/kjp.2014.57.6.292. Epub 2014 Jun 30.

3.

[Distal 1q monosomy. 2 new cases and description of the syndrome].

Turleau C, de Grouchy J, Frézal J, Richardet JM.

Ann Genet. 1983;26(3):161-4. French.

PMID:
6606378
4.

Further delineation of the dup(3q) syndrome.

Wilson GN, Dasouki M, Barr M Jr.

Am J Med Genet. 1985 Sep;22(1):117-23.

PMID:
4050847
5.

The phenotype of ring chromosome 3.

Wilson GN, Pooley J, Parker J.

J Med Genet. 1982 Dec;19(6):471-3.

6.

Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].

Al-Awadi SA, Farag TI, Usha R, el-Khalifa MY, Sundareshan TS, Al-Othman SA.

Am J Med Genet. 1986 Apr;23(4):931-3.

PMID:
3963055
7.

Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases.

Irving M, Hanson H, Turnpenny P, Brewer C, Ogilvie CM, Davies A, Berg J.

Am J Med Genet A. 2003 Dec 1;123A(2):153-63.

PMID:
14598339
8.

The 18p- syndrome. Report of five cases.

Zumel RM, Darnaude MT, Delicado A, Diaz de Bustamante A, de Torres ML, López-Pájares I.

Ann Genet. 1989;32(3):160-3.

PMID:
2817777
9.

Chromosome 10qter deletion syndrome: a review and report of three new cases.

Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL.

Am J Med Genet. 1989 Mar;32(3):364-7. Review.

PMID:
2658586
10.

Interstitial deletion of chromosome 1 (q23-q25). Report of a case.

Silengo MC, Davi GF, Bianco R, Biagioli M, Guala A, Franceschini P, Novelli G.

Clin Genet. 1984 Jun;25(6):549-52.

PMID:
6587954
11.

A specific syndrome due to deletion of the distal long arm of chromosome 1.

Meinecke P, Vögtel D.

Am J Med Genet. 1987 Oct;28(2):371-6. Review.

PMID:
3322005
12.

A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant.

Park JP, Moeschler JB, Berg SZ, Bauer RM, Wurster-Hill DH.

Clin Genet. 1992 Jan;41(1):54-6.

PMID:
1633649
13.

Familial partial trisomy of the long arm of chromosome 10 (q24-26).

Moreno-Fuenmayor H, Zackai EH, Mellman WJ, Aronson M.

Pediatrics. 1975 Nov;56(5):756-61.

PMID:
1196732
14.

De novo interstitial deletion del(1)(p21p32).

Bene M, Duca-Marinescu A, Ioan D, Maximilian C.

J Med Genet. 1979 Aug;16(4):323-7.

15.

Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature.

Sarda P, Lefort G, Taviaux S, Humeau C, Rieu D.

Clin Genet. 1992 Jan;41(1):25-7. Review.

PMID:
1633642
16.

Interstitial deletion of the long arm of chromosome 2: case report and review of literature.

Taysi K, Dengler DR, Jones LA, Heersma JR.

Ann Genet. 1981;24(4):245-7. Review. No abstract available.

PMID:
7036843
17.

Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.

Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J.

Am J Med Genet. 1988 Nov;31(3):533-48. Review.

PMID:
3067575
18.

The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature.

Torgyekes E, Shanske AL, Anyane-Yeboa K, Nahum O, Pirzadeh S, Blumfield E, Jobanputra V, Warburton D, Levy B.

Am J Med Genet A. 2011 Aug;155A(8):1884-96. doi: 10.1002/ajmg.a.34090. Epub 2011 Jul 8. Review.

PMID:
21744488
19.

Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.

Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B.

Ann Genet. 1992;35(4):208-12.

PMID:
1296516
20.

[Syndrome of terminal deletion of the long arm of chromosome 4. Apropos of a personal case with a review of the literature].

Frappaz D, Bourgeois J, Berthier JC, Laurent C, Bethenod M.

Pediatrie. 1983 Jun;38(4):261-70. Review. French.

PMID:
6353348
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