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Items: 1 to 20 of 187

1.

Craniosynostosis with Marfan syndrome, hand and foot anomalies.

Shah AM, Chattopadhyay A, Kher A, Bharucha BA, Karapurkar AP.

Clin Dysmorphol. 1996 Jul;5(3):263-6.

PMID:
8818457
2.

Newly recognized ectrodactyly/deafness syndrome.

Raas-Rothschild A, Aviram A, Ben-Ami T, Berger I, Katznelson MB, Goodman RM.

J Craniofac Genet Dev Biol. 1989;9(2):121-7.

PMID:
2794002
3.

Marfanoid features and craniosynostosis: report of one case and review.

Lacombe D, Battin J.

Clin Dysmorphol. 1993 Jul;2(3):220-4. Review.

PMID:
8287183
4.

[A case of congenital hypodactyly of the hand and foot].

Mamedov AG, Seidov MM.

Ortop Travmatol Protez. 1991 Apr;(4):51-2. Russian. No abstract available.

PMID:
1754179
5.

Hunter-McAlpine syndrome: report of a third family.

Ad├Ęs LC, Morris LL, Simpson DA, Haan EA.

Clin Dysmorphol. 1993 Apr;2(2):123-30.

PMID:
8281273
6.

Hand-foot-genital syndrome: the importance of hallux varus.

Cleveland RH, Holmes LB.

Pediatr Radiol. 1990;20(5):339-43.

PMID:
2349017
7.

Musculoskeletal manifestations of the Antley-Bixler syndrome.

Rumball KM, Pang E, Letts RM.

J Pediatr Orthop B. 1999 Apr;8(2):139-43. Review.

PMID:
10218180
8.

Postaxial polydactyly, ulnar ray dysgenesis, and renal cystic dysplasia in sibs.

Kaplan BS, Bellah RD.

Am J Med Genet. 1999 Dec 22;87(5):426-9.

PMID:
10594882
9.

Tibial hemimelia-split hand/foot syndrome with rare anomalies.

Managoli SS, Chaturvedi P.

Indian Pediatr. 2005 Feb;42(2):190-1. No abstract available.

10.

Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene.

Graham JM Jr, Braddock SR, Mortier GR, Lachman R, Van Dop C, Jabs EW.

Am J Med Genet. 1998 May 26;77(4):322-9.

PMID:
9600744
11.

Orthopaedic manifestations of Goldenhar syndrome.

Avon SW, Shively JL.

J Pediatr Orthop. 1988 Nov-Dec;8(6):683-6. Review.

PMID:
3056973
12.

An infant with multiple joint contractures.

Hou JW.

Acta Paediatr Taiwan. 2001 Mar-Apr;42(2):67-8. No abstract available.

PMID:
11355065
13.

Kaufman oculocerebrofacial syndrome in a girl of 15 years.

Briscioli V, Manoukian S, Selicorni A, Livini E, Lalatta F.

Am J Med Genet. 1995 Jul 31;58(1):21-3. Review.

PMID:
7573151
14.

Congenital cleft hand and cleft foot.

Patond KR, Kumar N, Srivastava SK.

Indian Pediatr. 1991 May;28(5):549-51. No abstract available.

PMID:
1752684
15.

Ectrodactyly, ectodermal dysplasia and clefting (EEC) syndrome.

Glorio R, Haas R, Jaimovich L.

J Eur Acad Dermatol Venereol. 2003 May;17(3):356-8. No abstract available.

PMID:
12702090
16.

An unusual case of Holt-Oram syndrome.

Mittal SR, Sethi A, Verma GL.

Int J Cardiol. 1984 Dec;6(6):740-2.

PMID:
6519847
17.

PHACE syndrome associated with club foot and thumb-in-palm deformity.

Lee SH, Kim JH, Lee JH, Kim SC.

J Dermatol. 2012 Dec;39(12):1054-5. doi: 10.1111/j.1346-8138.2012.01588.x. Epub 2012 Jun 1. No abstract available.

PMID:
22671438
18.

F-syndrome (F-form of acro-pectoro-vertebral dysplasia): report on a second family.

Camera G, Camera A, Pozzolo S, Costa M, Mantero R.

Am J Med Genet. 1995 Jul 3;57(3):472-5.

PMID:
7677153
19.

The Antley-Bixler syndrome: two new cases.

Hosalkar HS, Shah HS, Gujar PS, Shaw BA.

J Postgrad Med. 2001 Oct-Dec;47(4):252-5. Review.

20.

Anonychia and maxillofacial anomalies: an undefined syndrome?

Copcu E, Sivrioglu N, Oztan Y.

Ann Plast Surg. 2006 Mar;56(3):350-1. No abstract available.

PMID:
16508379

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