Two new Brazilian patients with Gómez-López-Hernández syndrome: Reviewing the expanded phenotype with molecular insights

American Journal of Medical Genetics, Part A

Volumn 146, Issue 5, 2008, Pages 649-657

  Gomy, Israel ^a   Heck, Benjamin ^a   Santos, Antônio Carlos ^a   Figueiredo, Maria Silvia L ^a   Martinelli Jr , Carlos E ^a   Nogueira, Maria Priscila C ^a   Pina Neto, João M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Acid phosphatase 2; Alopecia; Azygous anterior cerebral artery; Bipolar disorder; Growth hormone; Neurocutaneous disorder; Rhombencephalosynapsis

Indexed keywords

ACID PHOSPHATASE;

ADULT; ARTICLE; BIPOLAR DISORDER; BRAZIL; CASE REPORT; GOMEZ LOPEZ HERNANDEZ SYNDROME; GROWTH HORMONE DEFICIENCY; HUMAN; HYDROCEPHALUS; HYPOMANIA; HYPOPITUITARISM; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; MOLECULAR GENETICS; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SYNDROME; ALOPECIA; CEREBELLUM; CHILD; CONGENITAL MALFORMATION; GENETICS; GROWTH DISORDER; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PHAKOMATOSIS;

ABNORMALITIES, MULTIPLE; ADULT; ALOPECIA; BRAZIL; CEREBELLUM; CHILD; GROWTH DISORDERS; HUMANS; MALE; NEUROCUTANEOUS SYNDROMES; PHENOTYPE; SYNDROME;

EID: 43049142697     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32173     Document Type: Article

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