GENETICS OF HOLT-ORAM SYNDROME

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AKRAMI S.M.; AMIRI P.

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Journal: Iranian Journal of Pediatrics Year:2003 | Volume:13 | Issue:2 Page(s): 153-159

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Information Journal Paper

Title

GENETICS OF HOLT-ORAM SYNDROME

Author(s)

AKRAMI S.M. | AMIRI P. | Issue Writer Certificate

Keywords

HOLT-ORAM SYNDROMEQ4

AUTOSOMAL DOMINANTQ4

UPPER LIMB MALFORMATIONSQ4

CONGENITAL HEART MALFORMATIONSQ4

Abstract

HOLT-ORAM SYNDROME (HOS) is an AUTOSOMAL DOMINANT disorder, characterised by congenital heart and UPPER LIMB MALFORMATIONS. It is a rare disorder, however, there are several groups working on this syndrome worldwide since the genes involved in this syndrome are important to study on the cardiogenesis and development of hand.Although genetically heterogeneous, HOS is frequently linked to the TBX5 gene. To review the molecular genetics of HOS, this article has been written to highlight the importance of this syndrome and have more attention of pediatricians, cardiologists, heart surgeons, orthopedists and geneticists

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APA: Copy

AKRAMI, S.M., & AMIRI, P.. (2003). GENETICS OF HOLT-ORAM SYNDROME. IRANIAN JOURNAL OF PEDIATRICS, 13(2), 153-159. SID. https://sid.ir/paper/76121/en

Vancouver: Copy

AKRAMI S.M., AMIRI P.. GENETICS OF HOLT-ORAM SYNDROME. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2003;13(2):153-159. Available from: https://sid.ir/paper/76121/en

IEEE: Copy

S.M. AKRAMI, and P. AMIRI, “GENETICS OF HOLT-ORAM SYNDROME,” IRANIAN JOURNAL OF PEDIATRICS, vol. 13, no. 2, pp. 153–159, 2003, [Online]. Available: https://sid.ir/paper/76121/en

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