Myhre syndrome in a female with previously undescribed symptoms: Further delineation of the phenotype

American Journal of Medical Genetics, Part A

Volumn 139 A, Issue 2, 2005, Pages 127-130

  Van Steensel, M A M ^a   Vreeburg, M ^a   Steijlen, P M ^a   De Die Smulders, C ^a  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Hypertrophic scar; Myhre syndrome; Skin; Vertebral

Indexed keywords

ADOLESCENT; ANAMNESIS; APGAR SCORE; ARTICLE; BIRTH WEIGHT; BONE RADIOGRAPHY; CASE REPORT; CLINICAL FEATURE; ECHOCARDIOGRAPHY; FACIES; FEMALE; GESTATIONAL AGE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERTROPHIC SCAR; LABORATORY TEST; MYHRE RUVALCABA SYNDROME; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SKIN BIOPSY; SKIN DISEASE; SKIN EXAMINATION; SPINE DISEASE; SPINE FUSION; SYNDROME; ULTRASOUND; ABDOMEN; BONE; CONNECTIVE TISSUE DISEASE; ECHOGRAPHY; GENETICS; KARYOTYPING; PATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; RADIOGRAPHY;

ABDOMEN; BONE AND BONES; CONNECTIVE TISSUE DISEASES; ECHOCARDIOGRAPHY; FEMALE; HUMANS; KARYOTYPING; PHENOTYPE; SYNDROME;

EID: 33645851375     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.30988     Document Type: Article

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