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Items: 1 to 20 of 107

1.

Terminal 7p deletion and 1;7 translocation associated with craniosynostosis.

Dhadial RK, Smith MF.

Hum Genet. 1979 Sep;50(3):285-9.

PMID:
489013
2.

Interstitial deletion of the short arm of chromosome 7 without craniosynostosis.

Bianchi DW, Cirillo-Silengo M, Luzzatti L, Greenstein RM.

Clin Genet. 1981 Jun;19(6):456-61.

PMID:
7296937
3.

Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome.

Gong BT, Norwood TH, Hoehn H, McPherson E, Hall JG, Hickman R.

Hum Genet. 1976 Dec 29;35(1):117-23.

PMID:
1002161
4.

Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.

Aughton DJ, Cassidy SB, Whiteman DA, Delach JA, Guttmacher AE.

Am J Med Genet. 1991 Sep 15;40(4):440-3.

PMID:
1746608
5.

Partial deletion of distal 17q.

Bridge J, Sanger W, Mosher G, Buehler B, Nelson R, Welsh M, Newland J, Kafka M.

Am J Med Genet. 1985 Jun;21(2):225-9.

PMID:
4014309
6.

[7p-deletion syndrome].

Hinkel GK, Tolkendorf E, Bergan J.

Monatsschr Kinderheilkd. 1988 Dec;136(12):824-7. German.

PMID:
3237228
7.

The 9p- syndrome.

Alfi OS, Donnell GN, Allderdice PW, Derencsenyi A.

Ann Genet. 1976 Mar;19(1):11-6.

PMID:
1084115
8.

7p deletion syndrome: an adult with mild manifestations.

Grebe TA, Stevens MA, Byrne-Essif K, Cassidy SB.

Am J Med Genet. 1992 Sep 1;44(1):18-23.

PMID:
1519644
9.

De novo terminal deletion 7p22.1--pter in a child without craniosynostosis.

Speleman F, Craen M, Leroy J.

J Med Genet. 1989 Aug;26(8):528-32. Review.

10.

Partial duplication for the short arm of chromosome 2 : the 2p23 to pter syndrome.

Rosenfeld W, Verma RS, Jhaveri R, Dosik H, Evans H.

Ann Genet. 1982;25(1):28-31.

PMID:
6979296
11.

The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation.

Orye E, Verhaaren H, Van den Bogaert-Van Heesvelde AM.

Clin Genet. 1975 Nov;8(5):349-57.

PMID:
1204232
12.

[Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].

Siffroi JP, Romani F, Viguié F, Lejeune C.

Ann Genet. 1984;27(4):241-4. French.

PMID:
6335372
13.

Chromosome 7 short arm deletion, 7p21----pter.

Schömig-Spingler M, Schmid M, Brosi W, Grimm T.

Hum Genet. 1986 Nov;74(3):323-5.

PMID:
3781561
14.

Partial 3q trisomy due to an unbalanced 3/10 translocation.

Blumberg B, Moore R, Mohandas T.

Am J Med Genet. 1980;7(3):335-9.

PMID:
7468658
16.

A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21.

Motegi T, Ohuchi M, Ohtaki C, Fujiwara K, Enomoto S, Hasegawa T, Kishi K, Hayakawa H.

Hum Genet. 1985;71(2):160-2.

PMID:
4043965
17.

Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.

Larson LM, Wasdahl WA, Saumur JH, Coleman ML, Hall JG, Dolan CR, Schutta CJ.

Clin Genet. 1982 Mar;21(3):187-95.

PMID:
7094394
18.

Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocation.

Dennis NR, Neu RL, Bannerman RM.

Am J Med Genet. 1978;1(3):271-7.

PMID:
677166
19.

Developmental abnormalities associated with long arm deletion of chromosome No. 6.

Bartoshesky L, Lewis MB, Pashayan HM.

Clin Genet. 1978 Jan;13(1):68-71.

PMID:
624189
20.

Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.

Silengo MC, Luzzatti L, Centerwall WR, Costello JM, Parslow M.

Clin Genet. 1981 Mar;19(3):174-80.

PMID:
7273460

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