Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganization

American Journal of Medical Genetics, Part A

Volumn 149, Issue 8, 2009, Pages 1734-1739

  Isidor, B ^a   Baujat, G ^b   Le Caignec, C ^a,c   Pichon, O ^a   Martin Coignard, D ^d   Toutain, A ^e   David, A ^a  

^a NANTES UNIVERSITY HOSPITAL   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c L INSTITUT DU THORAX   (France)

^d Centre Hospitalier General   (France)

^e UNIVERSITY HOSPITAL OF TOURS   (France)

Author keywords

Amniotic band sequence; Congenital skin pedicle; Di George syndrome; Disorganization like syndrome

Indexed keywords

ABDOMINAL SCINTISCANNING; AMNION BAND; AMNION BAND SYNDROME; ANIMAL MODEL; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLEFT LIP; CLINICAL ARTICLE; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL SKIN DISEASE; CONGENITAL SKIN PEDICLE HAMARTOMATOUS; DIGEORGE SYNDROME; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; DISORIENTATION; ECHOGRAPHY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENE SEQUENCE; HUMAN; INFANT; KARYOTYPE 46,XX; KARYOTYPE 46,XY; KARYOTYPING; LIMB AMPUTATION; LIMB MALFORMATION; MALE; MICROARRAY ANALYSIS; MICRODELETION SYNDROME; MOUSE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SKIN DEFECT; SYNDACTYLY; X RAY;

AMNIOTIC BAND SYNDROME; ANIMALS; CHILD; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MICE; MICE, MUTANT STRAINS; PHENOTYPE; SKIN ABNORMALITIES;

EID: 68049094015     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32796     Document Type: Article

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