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Works matching Klein-Waardenburg syndrome

Results: 5

1

Waardenburg syndrome type 3 (Klein–Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?

Published in:

Clinical Genetics, 2001, v. 60, n. 4, p. 301, doi. 10.1034/j.1399-0004.2001.600408.x

By:

Tekin, M;
Bodurtha, JN;
Nance, WE;
Pandya, A

Publication type:

Article

2

Waardenburg syndrome: A report of three cases.

Published in:

Indian Journal of Dermatology, Venereology & Leprology, 2010, v. 76, n. 5, p. 550, doi. 10.4103/0378-6323.69089

By:

Ghosh, Sudip Kumar;
Bandyopadhyay, Debabrata;
Ghosh, Arghyaprasun;
Biswas, Surajit Kumar;
Mandal, Rajesh Kumar

Publication type:

Article

3

Biallelic variants in PAX3 cause Klein syndrome.

Published in:

Clinical Genetics, 2022, v. 102, n. 3, p. 223, doi. 10.1111/cge.14167

By:

Salah, Somaya;
Meiner, Vardiella;
Abumayaleh, Abdelrazzaq;
Asafra, Ali;
Al‐Sharif, Taher;
Al‐Fallah, Orwa;
Hasasneh, Belal;
Zlotogora, Joël

Publication type:

Article

4

Physiopathological investigations in a family with a history of unilateral hereditary deafness.

Published in:

1995

By:

Lina-Granade G;
Collet L;
Morgon A

Publication type:

Journal Article

5

Physiopathological Investigations in a Family with a History of Unilateral Mereditary Deafness.

Published in:

Acta Oto-Laryngologica, 1995, v. 115, n. 2, p. 196, doi. 10.3109/00016489509139291

By:

Lina-Granade, G.;
Collet, L.;
Morgon, A.

Publication type:

Article