نتایج جستجو برای: yunis

تعداد نتایج: 53  

Journal: :Journal of medical genetics 1969
S Kelly R Almy A Dagle

et al., 1961; Lubs, Koenig, and Brandt, 1961) has recently been identified with the late-replicating, distally labelled, D1 (13) pair (Yunis, Hook, and Mayer, 1964b; Yunis et al., 1964a; Yunis and Hook, 1966; Gianne]li, 1965; Giannelli and Howlett, 1966; Lee et al., 1966; Wilson et al., 1967; Bloom and Gerald, 1968). This report concerns a retarded adult with some manifestations of the D1 syndr...

Journal: :Acta medica Iranica 2014
Zahra Hadipour Yousef Shafeghati Fatemeh Hadipour

The Yunis-Varón syndrome represents a rare autosomal recessive syndrome of easy recognition characterized by defective growth of the cranial bone along with complete or partial absence of the clavicles (cleidocranial dysplasia), absence of thumbs and halluces, distal aphalangia, ectodermal anomalies, growth retardation and poor outcome. The molecular genetic basis is unknown. Here, we report an...

Journal: :Journal of medical genetics 1990
C Garrett A C Berry R H Simpson C M Hall

We report two male sibs and two female sibs from separate families, both with normal parents, who had a lethal condition with features of the Yunis-Varon syndrome and radiological signs of severe osteodysplasty. Autosomal recessive inheritance is likely in both families. The additional features described represent further delineation of the phenotype of the Yunis-Varon syndrome.

Journal: :Indian pediatrics 2005
Sameer Bhatia R G Holla

Yunis-Varon syndrome is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones along with complete or partial absence of the clavicles (cleidocranial dysplasia), characteristic facial features, and/or abnormalities of the fingers and/or toes.

Journal: :acta medica iranica 0
zahra hadipour department of medical genetics, sarem cell research center & hospital, tehran, iran. yousef shafeghati department of medical genetics, sarem cell research center & hospital, tehran, iran. and genetics research center, university of social welfare and rehabilitation sciences, tehran, iran. fatemeh hadipour department of medical genetics, sarem cell research center & hospital, tehran, iran.

the yunis-varón syndrome represents a rare autosomal recessive syndrome of easy recognition characterized by defective growth of the cranial bone along with complete or partial absence of the clavicles (cleidocranial dysplasia), absence of thumbs and halluces, distal aphalangia, ectodermal anomalies, growth retardation and poor outcome. the molecular genetic basis is unknown. here, we report an...

Journal: :Momentdergi 2021

This article explores the representation of masculinities in Alia Yunis’ The Night Counter and Shaila Abdullah`s Saffron Dreams. two novels I examine represent Arab-American Pakistani-American Muslim post-9/11 context. In first part, provide an overview research on Arab, Arab-American, Muslim, Pakistani after defining key terms. rest paper, trace representations novels. Yunis redeems Arab manho...

Journal: :Journal of Medical Genetics 1990

Journal: :World Journal of Current Medical and Pharmaceutical Research 2023

Yunis Varon Syndrome was first discovered by Emilio and Humberto in the year 1980. It affects both genders equal number. Most of infants are with Cleidocranial dysplasia, ectodermal anomalities, distal aphalangia. By characteristic features which including deformity pelvis, dislocation hips , bone fracture, urinary tract abnormalities, central nervous system abnormalities this they have reporte...

Journal: :Revista de Odontopediatría Latinoamericana 2021

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