These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 708615)

  • 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. PubMed ID: 708615
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Scalp-ear-nipple syndrome: additional manifestations.
    Edwards MJ; McDonald D; Moore P; Rae J
    Am J Med Genet; 1994 Apr; 50(3):247-50. PubMed ID: 8042668
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 1799422
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 9383029
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 134A(2):220-2. PubMed ID: 15712197
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Scalp-ear-nipple syndrome].
    Sonoda T
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):606-7. PubMed ID: 11528920
    [No Abstract]   [Full Text] [Related]  

  • 7. Breast reconstruction via fat grafting for a patient with bilateral congenital amastia (Finlay-Marks syndrome).
    Ito R; Yamamoto Y; Maeda T; Ishikawa K; Funayama E
    Congenit Anom (Kyoto); 2021 Jul; 61(4):142-143. PubMed ID: 33830564
    [No Abstract]   [Full Text] [Related]  

  • 8. 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. PubMed ID: 10517259
    [No Abstract]   [Full Text] [Related]  

  • 9. Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature.
    Butler KM; Bahrambeigi V; Merrihew A; Friez MJ; Cathey SS
    Clin Dysmorphol; 2021 Oct; 30(4):167-172. PubMed ID: 34456244
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 22639454
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lumpy scalp syndrome.
    Steinberg RD; Ethington J; Esterly NB
    Int J Dermatol; 1990 Nov; 29(9):657-8. PubMed ID: 2272740
    [No Abstract]   [Full Text] [Related]  

  • 12. 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;
    Am J Hum Genet; 2013 Apr; 92(4):621-6. PubMed ID: 23541344
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants.
    Smaldone G; Balasco N; Pirone L; Caruso D; Di Gaetano S; Pedone EM; Vitagliano L
    Sci Rep; 2019 Jul; 9(1):10519. PubMed ID: 31324836
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial occurrence of malformations possibly attributable to vascular abnormalities.
    Soltan HC; Holmes LB
    J Pediatr; 1986 Jan; 108(1):112-4. PubMed ID: 3944675
    [No Abstract]   [Full Text] [Related]  

  • 15. 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; 108(4):327-32. PubMed ID: 11920840
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Finlay-Marks syndrome: another sporadic case and additional manifestations.
    Taniai H; Chen H; Ursin S
    Pediatr Int; 2004 Jun; 46(3):353-5. PubMed ID: 15151556
    [No Abstract]   [Full Text] [Related]  

  • 17. Congenital defects of the breast - an autosomal dominant trait.
    Nelson MM; Cooper CK
    S Afr Med J; 1982 Mar; 61(12):434-6. PubMed ID: 7064019
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 140(3):300-2. PubMed ID: 16411189
    [No Abstract]   [Full Text] [Related]  

  • 19. 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. PubMed ID: 436331
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 991442
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.