10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies

American Journal of Medical Genetics, Part A

Volumn 167, Issue 11, 2015, Pages 2707-2713

  Choucair, Nancy ^a,b,c   Abou Ghoch, Joelle ^a   Fawaz, Ali ^d   Mégarbané, André ^a,e   Chouery, Eliane ^a  

^a SAINT JOSEPH UNIVERSITY   (Lebanon)

^b AIX MARSEILLE UNIVERSITY   (France)

^c INSERM   (France)

^d LEBANESE UNIVERSITY   (Lebanon)

^e Institute Jérôme Lejeune   (France)

Author keywords

Chromosomal microarray analysis; Critical region; Genital anomalies; Growth; Intellectual disability; Interstitial deletion; Microcephaly; Monosomy 10q; Psychomotor retardation

Indexed keywords

ARTICLE; ATE1 GENE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 10Q26; CLINICAL FEATURE; CRYPTORCHISM; EXOPHTHALMOS; FACE DYSMORPHIA; FGFR2 GENE; FLATFOOT; GENE; GENE DELETION; GRK5 GENE; HAPLOINSUFFICIENCY; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; KALLMANN SYNDROME; MALE; MICROARRAY ANALYSIS; MICROCEPHALY; MICROPENIS; NSMCEA4A GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; CHROMOSOME 10; COMPLICATION; DNA MICROARRAY; GENETICS; INFANT; NEWBORN; UROGENITAL TRACT MALFORMATION;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; HUMANS; INFANT; INFANT, NEWBORN; MALE; MICROCEPHALY; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; UROGENITAL ABNORMALITIES;

EID: 84946434638     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.37211     Document Type: Article

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