Author:
Lepri Francesca Romana,Scavelli Rossana,Digilio Maria Cristina,Gnazzo Maria,Grotta Simona,Dentici Maria Lisa,Pisaneschi Elisa,Sirleto Pietro,Capolino Rossella,Baban Anwar,Russo Serena,Franchin Tiziana,Angioni Adriano,Dallapiccola Bruno
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference42 articles.
1. Noonan JA: Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease. Am J Dis Child. 1968, 116: 373e380-
2. Nora JJ, Nora AH, Sinha AK, Spangler RD, Lubs HA: The Ullriche-Noonan syndrome (Turner phenotype). Am J Dis Child. 1974, 127: 48e55-
3. Gorlin RJ, Anderson RC, Blaw M: Multiples lentigienes syndrome syndrome. Am J Dis Child. 1969, 117: 652-662. 10.1001/archpedi.1969.02100030654006.
4. Reynolds JF, Neri G, Herrmann JP, Blumberg B, Coldwell JG, Miles PV, Opitz JM: New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement-the CFC syndrome. Am J Med Genet. 1986, 25 (3): 413-427. 10.1002/ajmg.1320250303.
5. Mazzanti L, Cacciari E, Cicognani A, Bergamaschi R, Scarano E, Forabosco A: Noonan-like syndrome with loose anagen hair: a new syndrome?. Am J Med Genet A. 2003, 118A (3): 279-286. 10.1002/ajmg.a.10923.
Cited by
58 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