نتایج جستجو برای: fryns

تعداد نتایج: 99  

2004
T Kleefstra H G Yntema A R Oudakker M J G Banning V M Kalscheuer J Chelly C Moraine C J Hamel H van Bokhoven

T Kleefstra, H G Yntema, A R Oudakker, M J G Banning, V M Kalscheuer, J Chelly, C Moraine, H-H Ropers, J-P Fryns, I M Janssen, E A Sistermans, W N Nillesen, L B A de Vries, B C J Hamel, H van Bokhoven . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ...

Journal: :Zootaxa 2014
Massimo Olmi Toshiharu Mita Adalgisa Guglielmino

Seven species of Embolemidae are recognized in Japan. They belong to two genera: Embolemus Westwood 1833 and Trogloembolemus Olmi, Mita et Guglielmino, gen. nov. (type species T. fujiei Olmi, Mita et Guglielmino, sp. nov.) Embolemus honshuensis Olmi, Mita et Guglielmino, sp. nov. (Japan, Honshu) and Trogloembolemus fujiei Olmi, Mita & Guglielmino, sp. nov. (Japan, Honshu) are described and figu...

Journal: :Pediatric and Developmental Pathology 2002

Journal: :Journal of medical genetics 1989
D P Cavalcanti

Young and Simpson in 1987 and Fryns and Moerman in 1988 each reported a case of a new unknown syndrome with hypothyroidism, severe global retardation, and abnormal facies, including microcephaly, blepharophimosis, bulbous nose, thin upper lip, low set ears, and micrognathia. A male infant with a similar pattern of malformations and postaxial polydactyly is reported here.

Journal: :Singapore medical journal 2007
A Pratap A Agrawal S Raja S Khaniya A Tiwari A Kumar

We report a pair of twins with variable expressions of Fryns syndrome, both of whom died in the neonatal period. The syndrome is characterised by craniofacial dysmorphism, diaphragmatic hernia and distal limb hypoplasia. With this report, there are a total of 83 cases reported in the literature and this further serves to illustrate the clinical variability of this disorder.

Journal: :genetics in the 3rd millennium 0
parva namiranian mehrvash shams alain verloes ariana kariminejad

fryns-aftimos syndrome is a rare autosomal dominant disorder characterized by craniofacial signs, anterior neuronal migration disorder (pachygyria, lissencephaly), skeletal deformities and mental retardation. we describe a five-year-old boy with abnormal facial features (hypertelorism, ptosis, high arched palate), skeletal problems (short stature, short fingers, flat feet) and mild intellectual...

Journal: :Ultrasound in Obstetrics and Gynecology 2008

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