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Results: 1 to 20 of 32

Related Articles by Review for PubMed (Select 6859126)

1.

Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.

Sommer A, Young-Wee T, Frye T.

Am J Med Genet. 1983 May;15(1):71-7.

PMID:
6859126
2.

Teebi hypertelorism syndrome: report of a third family.

Toriello HV, Delp K.

Clin Dysmorphol. 1994 Oct;3(4):335-9. Review.

PMID:
7894738
3.

Oto-palato-digital syndrome type II in two unrelated boys.

Preis S, Kemperdick H, Majewski F.

Clin Genet. 1994 Mar;45(3):154-61. Review.

PMID:
8026107
4.

The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.

Gollop TR, Fontes LR.

Am J Med Genet. 1985 Sep;22(1):59-68. Review.

PMID:
3901752
5.

Coffin-Lowry syndrome: clinical and molecular features.

Hanauer A, Young ID.

J Med Genet. 2002 Oct;39(10):705-13. Review.

6.

Autosomal dominant inheritance of the Aarskog syndrome.

Grier RE, Farrington FH, Kendig R, Mamunes P.

Am J Med Genet. 1983 May;15(1):39-46. Review.

PMID:
6344635
7.

Donnai-Barrow syndrome: four additional patients.

Chassaing N, Lacombe D, Carles D, Calvas P, Saura R, Bieth E.

Am J Med Genet A. 2003 Sep 1;121A(3):258-62. Review.

PMID:
12923867
8.

BBBG syndrome or Opitz syndrome: new family.

Verloes A, Le Merrer M, Briard ML.

Am J Med Genet. 1989 Nov;34(3):313-6. Review.

PMID:
2688419
9.

Aarskog syndrome: report of a family with review and discussion of nosology.

Teebi AS, Rucquoi JK, Meyn MS.

Am J Med Genet. 1993 Jun 15;46(5):501-9. Review.

PMID:
8322809
10.

Omodysplasia: an affected mother and son.

Venditti CP, Farmer J, Russell KL, Friedrich CA, Alter C, Canning D, Whitaker L, Mennuti MT, Driscoll DA, Zackai EH.

Am J Med Genet. 2002 Aug 1;111(2):169-77. Review.

PMID:
12210345
11.

Craniofrontonasal dysostosis with deafness and axillary pterygia.

Michels VV, Derleth DP, Hoffman AD, Goldston AS.

Am J Med Genet. 1989 Nov;34(3):445-50. Review.

PMID:
2688423
12.

Additional case of Keipert syndrome and review of the literature.

Cappon SM, Khalifa MM.

Med Sci Monit. 2000 Jul-Aug;6(4):776-8. Review.

13.

Neu-Laxova syndrome: pathological evaluation of a fetus and review of the literature.

King JA, Gardner V, Chen H, Blackburn W.

Pediatr Pathol Lab Med. 1995 Jan-Feb;15(1):57-79. Review.

PMID:
8736598
14.

Craniofacial manifestations of the amniotic band syndrome.

Bagatin M, Der Sarkissian R, Larrabee WF Jr.

Otolaryngol Head Neck Surg. 1997 Apr;116(4):525-8. Review. No abstract available.

PMID:
9141403
15.

New autosomal dominant branchio-oculo-facial syndrome.

Fujimoto A, Lipson M, Lacro RV, Shinno NW, Boelter WD, Jones KL, Wilson MG.

Am J Med Genet. 1987 Aug;27(4):943-51. Review.

PMID:
3321995
16.

Intrafamilial variability of Pfeiffer-type cardiocranial syndrome.

Digilio MC, Marino B, Borzaga U, Giannotti A, Dallapiccola B.

Am J Med Genet. 1997 Dec 31;73(4):480-3. Review.

PMID:
9415478
17.

Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosis.

Opitz JM, Mollica F, Sorge G, Milana G, Cimino G, Caltabiano M.

Am J Med Genet. 1993 Oct 1;47(5):660-78. Review.

PMID:
8266994
18.

Further case of aminopterin syndrome sine aminopterin in a Spanish child.

Garcia-Minaur S, Botella MP.

Am J Med Genet. 2000 Dec 11;95(4):320-4. Review.

PMID:
11186884
19.

Congenital hand anomaly: etiology and associated malformations.

Goldberg MJ, Bartoshesky LE.

Hand Clin. 1985 Aug;1(3):405-15. Review.

PMID:
3007544
20.

Freeman-Sheldon syndrome. A case report and review of the literature.

Ferrari D, Bettuzzi C, Donzelli O.

Chir Organi Mov. 2008 Sep;92(2):127-31. doi: 10.1007/s12306-008-0053-4. Epub 2008 Aug 1. Review.

PMID:
18677448
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