Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome-Reference-Cited by-同舟云学术

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

Published:2008-06-28 Issue:4 Volume:52 Page:231-234
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Plessis G.,Treust M. Le,Merrer M. Le

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02553.x/fullpdf

Reference21 articles.

1. The Finlay-Marks (SEN) syndrome: report of a new case and review of the literature;Aase;Proc Greenwood Genet Center,1988

2. Autosomal dominantly inherited cutis aplasia congenita, ear malformations, right-sided facial paresis, and dermal sinuses;Anderson;Birth Defects Original Article Series,1979

3. Scalp-ear-nipple syndrome: additional manifestations;Edwards;Am J Med Genet,1994

4. Aplasia cutis congenita and associated disorders: an update;Evers;Clin Genet,1995

5. An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples;Finlay;Br J Dermatol,1978

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. KCTD1 and Scalp-Ear-Nipple (‘Finlay–Marks’) syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains;Ophthalmic Genetics;2022-12-29

2. Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature;Clinical Dysmorphology;2021-08-26

3. AP-2β/KCTD1 Control Distal Nephron Differentiation and Protect against Renal Fibrosis;Developmental Cell;2020-08

4. Finlay-Marks Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

5. Finlay-Marks Syndrome;Atlas of Genetic Diagnosis and Counseling;2016