Johnson-McMillin syndrome, a neuroectodermal syndrome with conductive hearing loss and microtia: Report of a new case

American Journal of Medical Genetics

Volumn 120 A, Issue 3, 2003, Pages 400-405

  Schweitzer, Daniela N ^a   Yano, Shoji ^b   Earl, Dawn L ^a   Graham Jr , John M ^a,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^c CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

Alopecia; Cephalic neurocristopathy; Cleft palate; Developmental delay; Ectodermal dysplasia; Facial palsy; Hypogonadism; Hyposmia; Johnson McMillin syndrome; Microtia

Indexed keywords

ALOPECIA; ANOSMIA; ARTICLE; ATRESIA; AUDITORY CANAL ATRESIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHOANA ATRESIA; CHROMOSOME ANALYSIS; CLEFT PALATE; CLINICAL FEATURE; CONDUCTION DEAFNESS; CONGENITAL HEART DISEASE; DISEASE COURSE; ECTODERM; FACE MALFORMATION; FACIAL NERVE PARALYSIS; FALLOT TETRALOGY; FAMILY HISTORY; FEMALE; GROWTH RETARDATION; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; INTRAUTERINE GROWTH RETARDATION; JOHNSON MCMILLIN SYNDROME; MENTAL RETARDATION MALFORMATION SYNDROME; MICROCEPHALY; MICROTIA; NEUROECTODERM; PHENOTYPE; PHYSICAL EXAMINATION; POLYDACTYLY; PRIORITY JOURNAL; SEX RATIO;

GENETTA;

EID: 0041322498     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20085     Document Type: Article

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