The face of Ulnar Mammary syndrome?

European Journal of Medical Genetics

Volumn 54, Issue 3, 2011, Pages 301-305

  Joss, Shelagh ^a,e   Kini, Usha ^b   Fisher, Richard ^a   Mundlos, Stefan ^c   Prescott, Katrina ^a   Newbury Ecob, Ruth ^d   Tolmie, John ^e  

^a CHAPEL ALLERTON HOSPITAL   (United Kingdom)

^b The Churchill   (United Kingdom)

^c Institut fur Medizinische Genetik   (Germany)

^d ST MICHAEL'S HOSPITAL   (United Kingdom)

^e ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

Author keywords

Absent axillary hair; Delayed puberty; Fifth finger anomaly; Growth hormone deficiency; Polydactyly; Tongue tie

Indexed keywords

ADULT; AGED; ANKYLOGLOSSIA; ARTICLE; AUTOSOMAL DISORDER; BONE MALFORMATION; BREAST HYPOPLASIA; CHILD; CLINICAL ARTICLE; CLINODACTYLY; FEMALE; GENE; GENE MUTATION; GROWTH HORMONE DEFICIENCY; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYDROCELE; HYPERTRICHOSIS; INGUINAL HERNIA; MALE; NEWBORN; NIPPLE MALFORMATION; NOSE MALFORMATION; PALPEBRAL FISSURE ANOMALY; PHENOTYPE; PHOTOGRAPHY; POLYDACTYLY; PRESCHOOL CHILD; TBX3 GENE; TOOTH MALFORMATION; ULNAR MAMMARY SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; BREAST DISEASES; CHILD; CHILD, PRESCHOOL; FACE; FAMILY HEALTH; FEMALE; FINGERS; HUMANS; INFANT; MALE; MIDDLE AGED; MUTATION; PEDIGREE; SYNDROME; T-BOX DOMAIN PROTEINS; ULNA; YOUNG ADULT;

EID: 79955416254     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2010.12.010     Document Type: Article

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