Fetal phenotype associated with the 22q11 deletion

American Journal of Medical Genetics, Part A

Volumn 164, Issue 11, 2014, Pages 2724-2731

  Noël, Anne Claire ^a   Pelluard, Fanny ^b   Delezoide, Anne Lise ^c   Devisme, Louise ^d   Loeuillet, Laurence ^e   Leroy, Brigitte ^e   Martin, Alain ^f   Bouvier, Raymonde ^g   Laquerriere, Annie ^h   Jeanne Pasquier, Corinne ⁱ   Bessieres Grattagliano, Betty ^j   Mechler, Charlotte ^k   Alanio, Elisabeth ^a   Leroy, Camille ^a   Gaillard, Dominique ^a  

^a HÔPITAL MAISON BLANCHE   (France)

^b BORDEAUX UNIVERSITY HOSPITAL   (France)

^c HÔPITAL ROBERT DEBRÉ   (France)

^d LILLE UNIVERSITY HOSPITAL   (France)

^e CENTRE HOSPITALIER INTERCOMMUNAL   (France)

^f UNIVERSITY HOSPITAL OF BESANÇON   (France)

^g Centre de Biologie et Pathologie Est   (France)

^h ROUEN UNIVERSITY HOSPITAL   (France)

ⁱ Centre Hospitalier Universitaire   (France)

^j Institut de Puericulture   (France)

^k HÔPITAL LOUIS MOURIER   (France)

more..

Author keywords

22q11 deletion syndrome; Conotruncal cardiac defect; DiGeorge syndrome; Fetus; Holoprosencephaly; Kidney; Neural tube defect; Prenatal diagnosis; Thymus; Upper respiratory tract

Indexed keywords

ARTICLE; AUTOPSY; CHROMOSOME DELETION 22Q11; CONGENITAL HEART MALFORMATION; DISEASE ASSOCIATION; DISEASE SEVERITY; FEMALE; FETUS; FETUS DEATH; FETUS DISEASE; FIRST TRIMESTER PREGNANCY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC COUNSELING; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PREGNANCY TERMINATION; PRIORITY JOURNAL; SECOND TRIMESTER PREGNANCY; THIRD TRIMESTER PREGNANCY; THYMUS DISEASE; URINARY TRACT MALFORMATION; 22Q11 DELETION SYNDROME; ABNORMALITIES, MULTIPLE; ADULT; GENETIC ASSOCIATION STUDY; GENETICS; HEART DEFECTS, CONGENITAL; PREGNANCY; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDY;

22Q11 DELETION SYNDROME; ABNORMALITIES, MULTIPLE; ADULT; FEMALE; FETUS; GENETIC ASSOCIATION STUDIES; GENETIC COUNSELING; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PHENOTYPE; PREGNANCY; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDIES;

EID: 84910643092     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36720     Document Type: Article

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