Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 89

1.

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
2.
3.

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
4.

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. Review.

5.

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
6.

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.

7.

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
8.

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
10.

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
11.

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
12.
13.

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
15.

Aglossia-adactylia syndrome (special emphasis on the inheritance pattern).

Tuncbilek E, Yalcin C, Atasu M.

Clin Genet. 1977 Jun;11(6):421-3.

PMID:
880741
16.

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.

17.

Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.

Froster UG, Rehder H, Höhn W, Oberheuser F.

Am J Med Genet. 1993 Oct 1;47(5):717-22.

PMID:
8267003
19.

A new syndrome of broad terminal phalanges and facial abnormalities.

Keipert JA, Fitzgerald MG, Danks DM.

Aust Paediatr J. 1973 Feb;9(1):10-3. No abstract available.

PMID:
4708024
20.

Supplemental Content

Support Center