Familial deletion 18p syndrome: Case report

BMC Medical Genetics

Volumn 7, Issue , 2006, Pages

  Maranda, Bruno ^a   Lemieux, Nicole ^b   Lemyre, Emmanuelle ^a  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 18P SYNDROME; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; COGNITION; COGNITIVE DEFECT; CONTROLLED STUDY; DAUGHTER; DISEASE TRANSMISSION; FACE DYSMORPHIA; FAMILY STUDY; FEMALE; FEMALE FERTILITY; GENETIC COUNSELING; HUMAN; KARYOTYPE 46,XX; MENTAL DEFICIENCY; MENTAL PERFORMANCE; MOTHER; PSYCHOLOGIC ASSESSMENT; SCHOOL CHILD; SHORT STATURE; SPONTANEOUS ABORTION; TREATMENT OUTCOME; VERBAL BEHAVIOR;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; GROWTH DISORDERS; HUMANS; INTELLECTUAL DISABILITY; INTELLIGENCE TESTS; KARYOTYPING; SYNDROME;

EID: 33747290683     PISSN: 14712350     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-7-60     Document Type: Article

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