Pages that link to "Q34404983"

The following pages link to CHARGE syndrome: a review (Q34404983):

Displaying 25 items.

• The genetic landscape and clinical implications of vertebral anomalies in VACTERL association (Q26753049) (← links)
• Modeling congenital disease and inborn errors of development in Drosophila melanogaster (Q26765017) (← links)
• Tibial hemimelia: new classification and reconstructive options (Q28071839) (← links)
• Three novel mutations of CHD7 gene in two turkish patients with charge syndrome; A double point mutation and an insertion (Q36623495) (← links)
• Outcomes of long-term audiological rehabilitation in charge syndrome. (Q37158688) (← links)
• The Genetics Journey: A Case Report of a Genetic Diagnosis Made 30 Years Later (Q38557409) (← links)
• Chromatin remodeling and bivalent histone modifications in embryonic stem cells (Q38629414) (← links)
• Diversity in primary palate ontogeny of amniotes revealed with 3D imaging (Q39014957) (← links)
• CHARGE syndrome gastrointestinal involvement: from mouth to anus (Q39117190) (← links)
• Immunodeficiencies Associated with Abnormal Newborn Screening for T Cell and B Cell Lymphopenia (Q39206354) (← links)
• Spontaneous postnatal growth is reduced in children with CHARGE syndrome (Q41373833) (← links)
• Immunodeficiency associated with a nonsense mutation of IKBKB. (Q41741343) (← links)
• Newly Emerging Feeding Difficulties in a 33-Year-Old Adult With CHARGE Syndrome. (Q43134189) (← links)
• Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome (Q47222829) (← links)
• Pediatric Auditory Brainstem Implantation: Surgical, Electrophysiologic, and Behavioral Outcomes (Q47245852) (← links)
• Hearing loss and renal syndromes (Q47411095) (← links)
• Late Dumping Syndrome in a 17-Year-Old Female With Charge Syndrome (Q47569157) (← links)
• Genetic counseling in CHARGE syndrome: Diagnostic evaluation through follow up. (Q47867211) (← links)
• Gastrointestinal and feeding difficulties in CHARGE syndrome: A review from head-to-toe. (Q47870371) (← links)
• Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies (Q48093262) (← links)
• Developing a CHARGE syndrome checklist: Health supervision across the lifespan (from head to toe). (Q52731984) (← links)
• Neural crest contributions to the ear: Implications for congenital hearing disorders (Q62937932) (← links)
• Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants. (Q64905002) (← links)
• Hypogonadism and Cryptorchidism (Q89494701) (← links)
• Classification for treatment urgency for the microphthalmia/anophthalmia spectrum using clinical and biometrical characteristics (Q89888668) (← links)