New syndrome of mental retardation, Robin sequence, and brachydactyly

American Journal of Medical Genetics

Volumn 100, Issue 1, 2001, Pages 49-51

  Gurrieri, Fiorella ^a   Steindl, Katharina ^b   Giglio, Sabrina ^a   Neri, Giovanni ^b  

^a CATHOLIC UNIVERSITY   (Italy)

^b UNIVERSITY OF PAVIA   (Italy)

Author keywords

Cleft soft palate; New MCA MR syndrome; Robin sequence; Short digits

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRACHYDACTYLY; CASE REPORT; CLEFT PALATE; FACE MALFORMATION; FEMALE; HUMAN; MALE; MENTAL DEFICIENCY; PENETRANCE; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; FAMILY HEALTH; FEMALE; HAND DEFORMITIES, CONGENITAL; HUMANS; MALE; MENTAL RETARDATION; PIERRE ROBIN SYNDROME; SYNDROME;

RAPHIA FRATER;

EID: 0035871915     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010415)100:1<49::AID-AJMG1213>3.0.CO;2-V     Document Type: Article

References (4)

1. Velocardio-facial syndrome: A review of 120 patients
2. De Lange syndrome: A clinical review of 310 individuals
3. Perfect endings: A review of subtelomeric probes and their use in clinical diagnosis
4. Oral-facial-skeletal syndromes