larsen syndrome - Axtarish в Google
HamisiShekillerXeberlerVideolar
1 окт. 2019 г. · Larsen syndrome is a disorder that affects the development of bones throughout the body. The signs and symptoms of Larsen syndrome vary ...
Disease Overview. Summary. Larsen syndrome is a rare genetic disorder that has been associated with a wide variety of different symptoms.
16 июн. 2021 г. · Larsen's Syndrome is a rare genetic disorder caused by mutations in filamin B and carbohydrate sulfotransferase 3 deficiency, that presents ...
Larsen syndrome is a very rare genetic disorder that impacts the development of many of the bones in the body. The syndrome affects about 1 in 100000 babies ...
Larsen syndrome Болезнь или медицинское состояние
Синдром Ларсена — врожденное заболевание, открытое в 1950 году Ларсеном и его коллегами, когда они наблюдали вывих крупных суставов и аномалии лица у шести своих пациентов. Википедия (Английский язык)
Larsen syndrome (LS) is a congenital disorder discovered in 1950 by Larsen and associates when they observed dislocation of the large joints and face anomalies ...
Larsen syndrome is a disorder of the development of the bones. Signs and symptoms may include clubfoot and numerous joint dislocations at birth (affecting ...
An orofacial clefting syndrome characterized by congenital dislocation of large joints, foot deformities, cervical spine dysplasia, scoliosis, spatula-shaped ...
Larsen syndrome (LS) is a rare skeletal dysplasia characterized by congenital dislocation of large joints, foot deformities, cervical spine dysplasia, scoliosis ...
Larsen syndrome (LRS) is an osteochondrodysplasia characterized by large-joint dislocations and characteristic craniofacial abnormalities.
Novbeti >

 -  - 
Axtarisha Qayit
Anarim.Az


Anarim.Az

Sayt Rehberliyi ile Elaqe

Saytdan Istifade Qaydalari

Anarim.Az 2004-2023