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Items: 1 to 20 of 100

1.
2.

The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family.

Gollop TR, Colletto GM.

Am J Med Genet. 1984 Feb;17(2):399-406.

PMID:
6702893
3.

New manifestations observed in the Tel Hashomer camptodactyly syndrome.

Gollop T, Dal Colletto GM, Ferraretto I, Grimaldi A.

Prog Clin Biol Res. 1982;104:269-77. No abstract available.

PMID:
7163271
4.

The Tel Hashomer camptodactyly syndrome: report of a new case and review of the literature.

Pagnan NA, Gollop TR, Lederman H.

Am J Med Genet. 1988 Feb;29(2):411-7. Review.

PMID:
3281460
5.

Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family.

Tylki-Szymanska A.

Am J Med Genet. 1986 Mar;23(3):759-63.

PMID:
3953674
6.

Guadalajara camptodactyly syndrome type I. A corroborative family.

Figuera LE, Ramírez-Dueñas ML, García-Cruz D, Villar V, Cantú JM.

Clin Genet. 1993 Jan;43(1):11-5.

PMID:
7681735
7.

Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease.

Franceschini P, Vardeu MP, Signorile F, Testa A, Guala A, Franceschini D, Dalforno L.

Am J Med Genet. 1993 May 15;46(3):341-4. Review.

PMID:
8488882
8.

Tel Hashomer camptodactyly syndrome: report of a case with myopathic features.

Patton MA, McDermot KD, Lake BD, Baraitser M.

J Med Genet. 1986 Jun;23(3):268-71.

9.

The status of dermatoglyphics as a biomarker of Tel Hashomer camptodactyly syndrome: a review of the literature.

Wijerathne BT, Meier RJ, Agampodi SB.

J Med Case Rep. 2016 Sep 20;10(1):258. doi: 10.1186/s13256-016-1048-7.

11.

Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes.

Goodman RM, Katznelson MB, Manor E.

J Med Genet. 1972 Jun;9(2):203-12. No abstract available.

12.

Tel Hashomer camptodactyly syndrome: a case report.

Shah K, Sreekanth R, Thomas B, Danda S.

West Indian Med J. 2013 Jan;62(1):81-3.

PMID:
24171333
13.

The Coffin-Lowry syndrome: an inherited faciodigital mental retardation syndrome.

Temtamy SA, Miller JD, Hussels-Maumenee I.

J Pediatr. 1975 May;86(5):724-31.

PMID:
1133653
14.
15.

Syndactyly type V.

Robinow M, Johnson GF, Broock GJ.

Am J Med Genet. 1982 Apr;11(4):475-82.

PMID:
6283889
16.

Guadalajara camptodactyly syndrome type II.

Cantú JM, García-Cruz D, Gil-Viera J, Nazará Z, Ramírez ML, Solé-Pujol MT, Sánchez-Corona J.

Clin Genet. 1985 Jul;28(1):54-60.

PMID:
4040823
17.
18.
19.

Tel-Hashomer camptodactyly syndrome with hirsuitism in an Indian family.

Patel ZM, Adhia RA.

J Assoc Physicians India. 2004 Oct;52:837-8.

PMID:
15909866
20.
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