Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 149

1.
2.

Autopsy findings in a stillborn female infant with the Osebold-Remondini syndrome.

Opitz JM, Gilbert EF.

Am J Med Genet. 1985 Dec;22(4):811-9.

PMID:
4073129
3.

Grebe syndrome: clinical and radiographic findings in affected individuals and heterozygous carriers.

Costa T, Ramsby G, Cassia F, Peters KR, Soares J, Correa J, Quelce-Salgado A, Tsipouras P.

Am J Med Genet. 1998 Feb 17;75(5):523-9.

PMID:
9489798
4.

Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.

Kantaputra PN, Gorlin RJ, Langer LO Jr.

Am J Med Genet. 1992 Dec 1;44(6):730-7.

PMID:
1481840
5.

A case of mesomelic dysplasia Kantaputra type--new findings and a new diagnostic approach.

Siwicka KA, Kitoh H, Nishiyama M, Ishiguro N.

J Pediatr Orthop B. 2008 Sep;17(5):271-6. doi: 10.1097/BPB.0b013e32830cc3c8.

PMID:
19471182
7.

Brachydactylic multiple delta phalanges plus syndrome.

Ahn CP, Lachman RS, Cox VA, Blumberg B, Klein OD.

Am J Med Genet A. 2005 Sep 15;138(1):41-4.

PMID:
16092122
8.

A new nail dysplasia syndrome with onychonychia and absence and/or hypoplasia of distal phalanges.

Cooks RG, Hertz M, Katznelson MB, Goodman RM.

Clin Genet. 1985 Jan;27(1):85-91.

PMID:
3978841
9.

Oto-facio-osseous-gonadal syndrome: a new form of syndromic deafness?

da-Silva EO, Duarte AR, Lins TS.

Clin Genet. 1997 Jul;52(1):51-5.

PMID:
9272713
10.

A familial syndrome of short stature, deformities of the hands and feet, and an unusual facies.

Emery AE, Nelson MM.

J Med Genet. 1970 Dec;7(4):379-82. No abstract available.

11.

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
12.

Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance.

Faivre L, Le Merrer M, Baumann C, Polak M, Chatelain P, Sulmont V, Cousin J, Bost M, Cordier MP, Zackai E, Russell K, Finidori G, Pouliquen JC, Munnich A, Maroteaux P, Cormier-Daire V.

J Med Genet. 2001 Nov;38(11):745-9.

14.

Mutation of HOXA13 in hand-foot-genital syndrome.

Mortlock DP, Innis JW.

Nat Genet. 1997 Feb;15(2):179-80.

PMID:
9020844
15.

Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome.

Wieczorek D, Gillessen-Kaesbach G, Plewa S, Passarge E.

Clin Genet. 1996 Feb;49(2):98-102.

PMID:
8740922
16.

The split-hand and split-foot anomaly in a central African Negro population.

Viljoen DL, Beighton P.

Am J Med Genet. 1984 Nov;19(3):545-52.

PMID:
6507501
17.

A child with sclerocornea, short limbs, short stature, and distinct facial appearance.

Thompson EM, Winter RM.

Am J Med Genet. 1988 Jul;30(3):719-24. Review.

PMID:
3055984
18.
19.

[Tarsal-carpal coalition syndrome: a familial case].

Caino S, Dello Ruso B, Fano V, Obregón MG.

An Pediatr (Barc). 2012 Jun;76(6):355-9. doi: 10.1016/j.anpedi.2011.12.004. Epub 2012 Feb 9. Spanish.

20.

Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.

Saal HM, Greenstein RM, Weinbaum PJ, Poole AE.

Am J Med Genet. 1988 Jul;30(3):709-18.

PMID:
3189394

Supplemental Content

Support Center