Pallister-Killian syndrome: Rare phenotypic features and variable karyotypes

Balkan Journal of Medical Genetics

Volumn 11, Issue 2, 2008, Pages 65-68

  Liehr, Thomas ^a,e   Wegner, R D ^b   Stumm, M ^b   Joksic G ^c   Polityko, A ^d   Kosyakova, N ^a   Ewers, E ^a   Reich, D ^a   Wagner, R ^a   Weise, A ^a  

^a Institut fur Humangenetik und Anthropologie   (Germany)

^b Zentrum für Pränataldiagnostik   (Germany)

^c UNIVERSITY OF BELGRADE   (Serbia)

^d Republican Scientific Practical Centre Mother and Child   (Belarus)

^e Inst fur Humangenetik und A   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 10P; CHROMOSOME 12; CHROMOSOME ARM; ECHOGRAPHY; FACE MALFORMATION; FIBROBLAST; GESTATIONAL AGE; HUMAN; HUMAN TISSUE; HYPERPIGMENTATION; HYPOPIGMENTATION; ISOCHROMOSOME; KARYOTYPE; MATERNAL AGE; MENTAL DEFICIENCY; MORPHOLOGICAL TRAIT; MOSAICISM; OMPHALOCELE; PALLISTER KILLIAN SYNDROME; PHENOTYPE; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; SEIZURE; TETRASOMY; TRISOMY 12;

EID: 67549107825     PISSN: 13110160     EISSN: None     Source Type: Journal    
DOI: 10.2478/v10034-008-0023-z     Document Type: Article

References (8)

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