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Results: 1 to 20 of 174

1.

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
[PubMed - indexed for MEDLINE]
2.

Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.

Goodman RM, Katznelson MB, Hertz M, Katznelson A.

J Med Genet. 1976 Apr;13(2):136-41.

PMID:
933111
[PubMed - indexed for MEDLINE]
Free PMC Article
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
7.

Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: autosomal recessive entity?

Kilic I, Kilic BA, Ergin H, Aygün MG, Aksit MA.

Am J Med Genet. 1998 Apr 28;77(1):28-30.

PMID:
9557890
[PubMed - indexed for MEDLINE]
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.

PMID:
3723560
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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
[PubMed - indexed for MEDLINE]
10.

Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.

Miny P, Lenz W.

Am J Med Genet. 1985 Jun;21(2):317-24.

PMID:
4014313
[PubMed - indexed for MEDLINE]
11.

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
[PubMed - indexed for MEDLINE]
12.

Mesomelic limb shortness: a previously unreported autosomal recessive type.

Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM.

Am J Med Genet. 1993 Oct 1;47(5):788-92.

PMID:
8267013
[PubMed - indexed for MEDLINE]
13.

Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.

Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.

Am J Med Genet. 1992 Jan 1;42(1):112-6.

PMID:
1308349
[PubMed - indexed for MEDLINE]
14.

[The Tel Hashomer camptodactyly syndrome].

Rogovina EG, Aver'ianov IuN, Nechkina NP, Logunova LV.

Zh Nevrol Psikhiatr Im S S Korsakova. 1995;95(4):83-6. Review. Russian.

PMID:
8533519
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

A probably distinct autosomal recessive thoraco-limb dysplasia.

Rivera H, Perez-Salas JM, Nazara Z, Ramirez ML.

J Med Genet. 1988 Sep;25(9):619-22.

PMID:
3184141
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian family.

Richieri-Costa A, Brunoni D, Laredo Filho J, Kasinski S.

Am J Med Genet. 1987 Dec;28(4):971-80.

PMID:
3688036
[PubMed - indexed for MEDLINE]
18.
19.

Pathologic features in two siblings with the Pena-Shokeir I syndrome.

Bisceglia M, Zelante L, Bosman C, Cera R, Dallapiccola B.

Eur J Pediatr. 1987 May;146(3):283-7.

PMID:
3595647
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]
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