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Consequences of chromsome18q deletions
Jannine D. Cody
, Courtney Sebold
, Patricia Heard
, Erika Carter
, Bridgette Soileau
, Minire Hasi-Zogaj
, Annice Hill
, David Rupert
, Brian Perry
, Louise O'donnell
,
Jon Gelfond
, Jack Lancaster
,
Peter T. Fox
, Daniel E. Hale
Department of Pediatrics
Division of Endocrinology
Research output
:
Contribution to journal
›
Article
›
peer-review
49
Scopus citations
Overview
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Medicine and Dentistry
Gene
100%
Phenotype
50%
Myelin Deficiency
33%
Persistent Truncus Arteriosus
33%
Bone Morphology
33%
Therapeutic Procedure
33%
Comprehension
33%
Person
33%
Syndrome
33%
Diseases
16%
Central Nervous System
16%
Mood Disorder
16%
Growth Hormone Deficiency
16%
Genotype
16%
Heredity
16%
Strabismus
16%
Corpus Callosum
16%
Executive Function
16%
Reflux
16%
Sensorineural Hearing Loss
16%
Haploinsufficiency
16%
Perivascular Space
16%
Speech Delay
16%
Atresia
16%
Kidney Malformation
16%
Hemizygosity
16%
Talus
16%
Polyposis
16%
Funnel Chest
16%
Cleft Palate
16%
Intellectual Disability
16%
Male Infertility
16%
Immunoglobulin A Deficiency
16%
Nystagmus
16%
Prognosis
16%
Biochemistry, Genetics and Molecular Biology
Nested Gene
100%
Phenotype
50%
Comprehension
33%
Genotyping
16%
Mental Retardation
16%
Genetic Determinism
16%
Haploinsufficiency
16%
Hemizygosity
16%
Excavata
16%
Executive Function
16%
Growth Hormone
16%
Hearing
16%
DNA
16%
Speech
16%
Mood
16%
Immunoglobulin A
16%