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Results: 1 to 20 of 127

1.

An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples.

Finlay AY, Marks R.

Br J Dermatol. 1978 Oct;99(4):423-30.

PMID:
708615
[PubMed - indexed for MEDLINE]
2.

Scalp-ear-nipple syndrome: additional manifestations.

Edwards MJ, McDonald D, Moore P, Rae J.

Am J Med Genet. 1994 Apr 15;50(3):247-50.

PMID:
8042668
[PubMed - indexed for MEDLINE]
3.

Scalp defect, nipples absence and ears abnormalities: an other case of Finlay syndrome.

Le Merrer M, Renier D, Briard ML.

Genet Couns. 1991;2(4):233-6.

PMID:
1799422
[PubMed - indexed for MEDLINE]
4.

Hypothelia, syndactyly, and ear malformation--a variant of the scalp-ear-nipple syndrome?: Case report and review of the literature.

Baris H, Tan WH, Kimonis VE.

Am J Med Genet A. 2005 Apr 15;134A(2):220-2. Review. Erratum in: Am J Med Genet A. 2005 Jul 1;136(1):114-5.

PMID:
15712197
[PubMed - indexed for MEDLINE]
5.

Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome.

Plessis G, Le Treust M, Le Merrer M.

Clin Genet. 1997 Oct;52(4):231-4. Review.

PMID:
9383029
[PubMed - indexed for MEDLINE]
6.

[Scalp-ear-nipple syndrome].

Sonoda T.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):606-7. Review. Japanese. No abstract available.

PMID:
11528920
[PubMed - indexed for MEDLINE]
7.

Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvement.

Picard C, Couderc S, Skojaei T, Salomon R, de Lonlay P, Le Merrer M, Munnich A, Lyonnet S, Amiel J.

Clin Genet. 1999 Aug;56(2):170-2. Review. No abstract available.

PMID:
10517259
[PubMed - indexed for MEDLINE]
8.

Scalp defects, polythelia, microcephaly, and developmental delay: a new syndrome with apparent autosomal dominant inheritance.

Marble M, Pridjian G.

Am J Med Genet. 2002 Apr 1;108(4):327-32.

PMID:
11920840
[PubMed - indexed for MEDLINE]
9.

Lumpy scalp syndrome.

Steinberg RD, Ethington J, Esterly NB.

Int J Dermatol. 1990 Nov;29(9):657-8. No abstract available.

PMID:
2272740
[PubMed - indexed for MEDLINE]
10.

Finlay-Marks syndrome: report of two siblings and review of literature.

Naik P, Kini P, Chopra D, Gupta Y.

Am J Med Genet A. 2012 Jul;158A(7):1696-701. doi: 10.1002/ajmg.a.35389. Epub 2012 May 25. Review.

PMID:
22639454
[PubMed - indexed for MEDLINE]
11.

Familial occurrence of malformations possibly attributable to vascular abnormalities.

Soltan HC, Holmes LB.

J Pediatr. 1986 Jan;108(1):112-4. No abstract available.

PMID:
3944675
[PubMed - indexed for MEDLINE]
12.

Genetic studies in a family with inverted nipples (mammillae invertita).

Shafir R, Bonne-Tamir B, Ashbel S, Tsur H, Goodman RM.

Clin Genet. 1979 Apr;15(4):346-50.

PMID:
436331
[PubMed - indexed for MEDLINE]
13.

Mutations in KCTD1 cause scalp-ear-nipple syndrome.

Marneros AG, Beck AE, Turner EH, McMillin MJ, Edwards MJ, Field M, de Macena Sobreira NL, Perez AB, Fortes JA, Lampe AK, Giovannucci Uzielli ML, Gordon CT, Plessis G, Le Merrer M, Amiel J, Reichenberger E, Shively KM, Cerrato F, Labow BI, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics.

Am J Hum Genet. 2013 Apr 4;92(4):621-6. doi: 10.1016/j.ajhg.2013.03.002. Epub 2013 Mar 28.

PMID:
23541344
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Aberrant axillary breast tissue: A report of a family with six affected women in two generations.

Weinberg SK, Motulsky AG.

Clin Genet. 1976 Dec;10(6):325-8.

PMID:
991442
[PubMed - indexed for MEDLINE]
15.

Finlay-Marks syndrome: another sporadic case and additional manifestations.

Taniai H, Chen H, Ursin S.

Pediatr Int. 2004 Jun;46(3):353-5. Review. No abstract available.

PMID:
15151556
[PubMed - indexed for MEDLINE]
16.

The ulnar-mammary syndrome: an autosomal dominant pleiotropic gene.

Schinzel A, Illig R, Prader A.

Clin Genet. 1987 Sep;32(3):160-8. Erratum in: Clin Genet 1987 Dec;32(6):425.

PMID:
3621662
[PubMed - indexed for MEDLINE]
17.

Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndrome.

Sobreira NL, Brunoni D, Cernach MC, Perez AB.

Am J Med Genet A. 2006 Feb 1;140(3):300-2. No abstract available.

PMID:
16411189
[PubMed - indexed for MEDLINE]
18.

LADD syndrome: report of new cases and review of the clinical spectrum.

Wiedemann HR, Drescher J.

Eur J Pediatr. 1986 Apr;144(6):579-82.

PMID:
3709571
[PubMed - indexed for MEDLINE]
19.

The deafness, pre-auricular sinus, external ear anomaly and commissural lip pits syndrome--otological, vestibular and radiological findings.

Marres HA, Cremers CW, Huygen PL, Joosten FB.

J Laryngol Otol. 1994 Jan;108(1):13-8.

PMID:
8133157
[PubMed - indexed for MEDLINE]
20.

Autosomal dominant inheritance of scalp defects with ectrodactyly.

Bonafede RP, Beighton P.

Am J Med Genet. 1979;3(1):35-41.

PMID:
474617
[PubMed - indexed for MEDLINE]
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