Trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies, and hypotonia in sibs

Author:

Teebi Ahmad S.

Publisher

Wiley

Subject

Genetics (clinical)

Reference6 articles.

1. Further delineation of the C (trigonocephaly) syndrome

2. A new X-linked mental retardation-overgrowth syndrome

3. (1988): “Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive and X-Linked Phenotypes,” 8th Ed. Baltimore: The Johns Hopkins University Press.

4. (1979): “C Syndrome. Birth Defects Compendium,” ed. 2. New York: Alan R. Liss, Inc., pp 160-161.

5. Diagnosis of chromosome 3 duplication q23→qter, deletion p25→pter in a patient with the C (trigonocephaly) syndrome

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1. Genetic Disorders in Kuwait;Genetic Disorders Among Arab Populations;2010

2. Genetic Disorders Among the Palestinians;Genetic Disorders Among Arab Populations;2010

3. New Syndromes First Reported Among Arabs;Genetic Disorders Among Arab Populations;2010

4. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

5. Clinical and genetic aspects of trigonocephaly: A study of 25 cases;American Journal of Medical Genetics Part A;2002-11-25

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