Familial Poland anomaly revisited

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 1, 2012, Pages 140-149

  Baban, Anwar ^a,b   Torre, Michele ^b   Costanzo, Sara ^b   Gimelli, Stefania ^c   Bianca, Sebastiano ^d   Divizia, Maria Teresa ^b   Sénès, Filippo Maria ^b   Garavelli, Livia ^e   Rivieri, Francesca ^e   Lerone, Margherita ^b   Valle, Maura ^b   Ravazzolo, Roberto ^b,f   Calevo, Maria Grazia ^b  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b G GASLINI INSTITUTE   (Italy)

^c GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^d ARNAS Garibaldi Nesima   (Italy)

^e S MARIA NUOVA HOSPITAL   (Italy)

^f UNIVERSITY OF GENOA   (Italy)

Author keywords

16q23.1 duplication; Familial Poland anomaly (F PA); Poland anomaly (PA); Sporadic

Indexed keywords

ADOLESCENT; ADULT; ARM MALFORMATION; CHILD; CHROMOSOME 1; CHROMOSOME 16Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME XP; CLINICAL FEATURE; COHORT ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; FAMILIAL DISEASE; FEMALE; GENETIC COUNSELING; HUMAN; INFANT; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; MICROARRAY ANALYSIS; MOLECULAR DYNAMICS; MUSCLE DISEASE; PECTORAL MUSCLE; PHYSICAL EXAMINATION; POLAND SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; RECURRENCE RISK; REVIEW; SCHOOL CHILD; SEX RATIO; VERTICAL TRANSMISSION;

CHILD; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; DNA; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC COUNSELING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PECTORALIS MUSCLES; PEDIGREE; POLAND SYNDROME;

EID: 84455202355     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34370     Document Type: Review

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