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Results: 1 to 20 of 206

1.

Hemifacial microsomia and variants: pedigree data.

Rollnick BR, Kaye CI.

Am J Med Genet. 1983 Jun;15(2):233-53.

PMID:
6881197
[PubMed - indexed for MEDLINE]
2.

Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients.

Rollnick BR, Kaye CI, Nagatoshi K, Hauck W, Martin AO.

Am J Med Genet. 1987 Feb;26(2):361-75.

PMID:
3812588
[PubMed - indexed for MEDLINE]
3.

Craniovertebral malformations in hemifacial microsomia.

Figueroa AA, Friede H.

J Craniofac Genet Dev Biol Suppl. 1985;1:167-78.

PMID:
3877093
[PubMed - indexed for MEDLINE]
4.

Malformations of the auricle: isolated and in syndromes. IV. Cumulative pedigree data.

Kaye CI, Rollnick BR, Pruzansky S.

Birth Defects Orig Artic Ser. 1979;15(5C):163-9. No abstract available.

PMID:
526600
[PubMed - indexed for MEDLINE]
5.

Hemifacial microsomia and the branchio-oto-renal syndrome.

Rollnick BR, Kaye CI.

J Craniofac Genet Dev Biol Suppl. 1985;1:287-95.

PMID:
3877103
[PubMed - indexed for MEDLINE]
6.

A comparison of microtia and temporal bone anomalies in hemifacial microsomia and mandibulofacial dysostosis.

Caldarelli DD, Hutchinson JG Jr, Pruzansky S, Valvassori GE.

Cleft Palate J. 1980 Apr;17(2):103-10.

PMID:
6929227
[PubMed - indexed for MEDLINE]
7.

Familial hemifacial microsomia due to autosomal dominant inheritance. Case reports.

Singer SL, Haan E, Slee J, Goldblatt J.

Aust Dent J. 1994 Oct;39(5):287-91.

PMID:
7811205
[PubMed - indexed for MEDLINE]
8.

Syndromic ear anomalies and renal ultrasounds.

Wang RY, Earl DL, Ruder RO, Graham JM Jr.

Pediatrics. 2001 Aug;108(2):E32.

PMID:
11483842
[PubMed - indexed for MEDLINE]
9.

A family with dominant oculoauriculovertebral spectrum.

Stoll C, Viville B, Treisser A, Gasser B.

Am J Med Genet. 1998 Jul 24;78(4):345-9.

PMID:
9714437
[PubMed - indexed for MEDLINE]
10.

[Familial occurrence of oculoauricolovertebral dysplasia and Franceschetti syndrome].

Bestelmeyer U, Weerda H, Siegert R, Greiwe M, Schwinger E.

HNO. 1996 Aug;44(8):452-5. German.

PMID:
8805011
[PubMed - indexed for MEDLINE]
11.

Goldenhar syndrome and hemifacial microsomia: observations on three patients.

Thomas P.

Eur J Pediatr. 1980 May;133(3):287-92.

PMID:
7389743
[PubMed - indexed for MEDLINE]
12.

Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum.

Johnson JP, Poskanzer LS, Sherman S.

Am J Med Genet. 1996 Jan 11;61(2):134-9.

PMID:
8669439
[PubMed - indexed for MEDLINE]
13.

Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.

Ng YY, Hu JM, Su PH, Chen JY, Yang MS, Chen SJ.

Acta Paediatr Taiwan. 2006 May-Jun;47(3):142-5.

PMID:
17078468
[PubMed - indexed for MEDLINE]
14.

Thrombophilia gene mutations in oculoauriculovertebral spectrum.

Tug E, Atasoy HI, Koybasi Sanal S.

Genet Couns. 2012;23(1):65-72.

PMID:
22611644
[PubMed - indexed for MEDLINE]
15.

Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q).

Herman GE, Greenberg F, Ledbetter DH.

Am J Med Genet. 1988 Apr;29(4):909-15.

PMID:
3400736
[PubMed - indexed for MEDLINE]
16.

Microtia: a clinical and genetic study at the National Institute of Pediatrics in Mexico City.

Llano-Rivas I, González-del Angel A, del Castillo V, Reyes R, Carnevale A.

Arch Med Res. 1999 Mar-Apr;30(2):120-4.

PMID:
10372445
[PubMed - indexed for MEDLINE]
17.

Familial hemifacial microsomia.

Taysi K, Marsh JL, Wise DM.

Cleft Palate J. 1983 Jan;20(1):47-53.

PMID:
6572575
[PubMed - indexed for MEDLINE]
18.

[Oto-mandibular dysplasias: genetics and nomenclature of syndromes].

Burglen L, Soupre V, Diner PA, Gonzalès M, Vazquez MP.

Ann Chir Plast Esthet. 2001 Oct;46(5):400-9. French.

PMID:
11770450
[PubMed - indexed for MEDLINE]
19.

Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature.

Vendramini S, Richieri-Costa A, Guion-Almeida ML.

Eur J Hum Genet. 2007 Apr;15(4):411-21. Epub 2007 Feb 7. Review.

PMID:
17290277
[PubMed - indexed for MEDLINE]
Free Article
20.

Dysmorphogenesis of the mandible, zygoma, and middle ear ossicles in hemifacial microsomia and mandibulofacial dysostosis.

Kay ED, Kay CN.

Am J Med Genet. 1989 Jan;32(1):27-31.

PMID:
2705480
[PubMed - indexed for MEDLINE]

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