Smith-Magenis Syndrome: Report of Two Cases and Review of the Literature

Author:

Al-Qudah AbdelKarim A.1,El-Khateeb Mohammed S.1,Abu-Hamour Walid1,Bulos Najwa Khoury1

Affiliation:

1. From the Departments of Pediatrics (Drs. Al-Qudah, Abu-Hamour and Bulos) and Cytogenetic Lab (Dr. El-Khateeb), Faculty of Medicine, University of Jordan, Amman

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference19 articles.

1. Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del (17) (p 11.2);Greenberg F;Am J Hum Genet,1991

2. Clinical and chromosome studies of three patients with Smith-Magenis syndrome;de-Rikik-Van-Andel JF;Dev Med Child Neur,1991

3. Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases;Moncla A;J Med Genet,1991

4. Interstitial deletion of (17) (P 11.2, P 11.2) in nine patients;Smith ACM;Am J Med Genet,1986

5. Interstitial deletion of short arm of chromosome 17;Patil SR;Hum Genet,1984

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