The purpose of this study was to clarify the prevalence, type, severity, and age-dependency of hearing loss in 22q11.2 deletion syndrome.status: publishe
The article presents own clinical observation of the chromosome 22q11.2 microdeletion syndrome in a ...
The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22. 2...
Background: Guanine deletion 35delG in GJB2 exon 2 is the pathogenic mutation responsible for up to ...
Background: Hearing loss and otitis media are frequently reported in patients with 22q11.2 deletion ...
Hearing loss is frequently present in the 22q11.2 deletion syndrome. Our aim was to describe the aud...
The 22q11.2 deletion syndrome is a common genetic disorder that affects for example the heart, palat...
Studies of geriatric, profoundly deaf, and syndromic hearing-loss populations demonstrate significan...
The 22q11.2 deletion syndrome (22q11.2DS) is the second most common cause of developmental delay aft...
22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of th...
Purpose: 22q11.2 deletion syndrome is a contiguous gene deletion syndrome with multisystem involveme...
22q11.2 deletion syndrome (22q11DS), most frequently caused by a de novo microdeletion on the long a...
To investigate the clinical manifestations at diagnosis and during follow-up in patients with 22q11....
Contains fulltext : 47828.pdf (publisher's version ) (Closed access)Hearing impair...
Laura M Dominguez, Kelley M DodsonDepartment of Otolaryngology, Head and Neck Surgery, Virginia Comm...
The 22q11 deletion syndrome (22q11DS), the most frequent microdeletion syndrome in humans, presents ...
The article presents own clinical observation of the chromosome 22q11.2 microdeletion syndrome in a ...
The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22. 2...
Background: Guanine deletion 35delG in GJB2 exon 2 is the pathogenic mutation responsible for up to ...
Background: Hearing loss and otitis media are frequently reported in patients with 22q11.2 deletion ...
Hearing loss is frequently present in the 22q11.2 deletion syndrome. Our aim was to describe the aud...
The 22q11.2 deletion syndrome is a common genetic disorder that affects for example the heart, palat...
Studies of geriatric, profoundly deaf, and syndromic hearing-loss populations demonstrate significan...
The 22q11.2 deletion syndrome (22q11.2DS) is the second most common cause of developmental delay aft...
22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of th...
Purpose: 22q11.2 deletion syndrome is a contiguous gene deletion syndrome with multisystem involveme...
22q11.2 deletion syndrome (22q11DS), most frequently caused by a de novo microdeletion on the long a...
To investigate the clinical manifestations at diagnosis and during follow-up in patients with 22q11....
Contains fulltext : 47828.pdf (publisher's version ) (Closed access)Hearing impair...
Laura M Dominguez, Kelley M DodsonDepartment of Otolaryngology, Head and Neck Surgery, Virginia Comm...
The 22q11 deletion syndrome (22q11DS), the most frequent microdeletion syndrome in humans, presents ...
The article presents own clinical observation of the chromosome 22q11.2 microdeletion syndrome in a ...
The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22. 2...
Background: Guanine deletion 35delG in GJB2 exon 2 is the pathogenic mutation responsible for up to ...