Catel-Manzke syndrome: A clinical report suggesting autosomal recessive inheritance

American Journal of Medical Genetics, Part A

Volumn 155, Issue 9, 2011, Pages 2288-2292

  Kiper, Pelin Özlem Şimşek ^a   Utine, Gülen Eda ^a   Boduroǧlu, Koray ^a   Alanay, Yasemin ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Autosomal recessive inheritance; Catel Manzke syndrome; Cleft palate; Pierre Robin sequence

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BONE RADIOGRAPHY; CASE REPORT; CATEL MANZKE SYNDROME; CLEFT PALATE; CLINICAL FEATURE; CLINODACTYLY; CYANOSIS; DISEASE ASSOCIATION; DYSPNEA; FINGER MALFORMATION; HEART MURMUR; HEART SEPTUM DEFECT; HUMAN; INFANT; JOINT LAXITY; MALE; METACARPOPHALANGEAL JOINT; MOTOR CONTROL; PATENT DUCTUS ARTERIOSUS; PHYSICAL EXAMINATION; PIGEON THORAX; PRIORITY JOURNAL; RETROGNATHIA; SCOLIOSIS;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOME DISORDERS; CLEFT PALATE; CONSANGUINITY; FEMALE; GENES, RECESSIVE; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT; MALE; PIERRE ROBIN SYNDROME;

EID: 81155160846     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34163     Document Type: Article

References (11)

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