A new multiple malformation syndrome of Mullerian dysgenesis and conductive hearing loss with facial hypoplasia, bilateral forearm deformity, brachydactyly, spinal stenosis and scoliosis

Clinical Genetics

Volumn 52, Issue 1, 1997, Pages 30-36

  Kumar, D ^a   Masel, J P ^b  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Brachydactyly; Congenital malformation syndrome; Deafness; Facial dysmorphism; Limb deformity; Mullerian dysgenesis; Scoliosis; Vertebral anomaly

Indexed keywords

ADULT; ARM MALFORMATION; ARTICLE; BRACHYDACTYLY; CASE REPORT; CONDUCTION DEAFNESS; FACE ASYMMETRY; FACE DYSMORPHIA; FACE MALFORMATION; FEMALE; FOREARM; GONADAL DYSGENESIS; HUMAN; HYPOPLASIA; KYPHOSCOLIOSIS; MEDICAL GENETICS; MUELLERIAN DUCT; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; SCOLIOSIS; SKELETON MALFORMATION; UROGENITAL SINUS; VERTEBRAL CANAL STENOSIS;

ILIA;

EID: 0030837552     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02511.x     Document Type: Article

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