Results 111 to 120 of about 1,354,450 (122)

Immunologic defects in 22q11.2 deletion syndrome

Journal of Allergy and Clinical Immunology, 2008
Andrew Gennery, Andrew Mclean-Tooke, Dawn Barge   +2 more
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The Genetics and Epigenetics of 22q11.2 Deletion Syndrome

Frontiers in Genetics, 2020
Nicolai van Oers, De la Morena M Teresa   +1 more
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Risk of malignancy in 22q11.2 deletion syndrome

Clinical Case Reports (discontinued), 2017
Machiel van den Akker
exaly  

22q11.2 deletion syndrome in diverse populations

American Journal of Medical Genetics, Part A, 2017
Antonio R Porras, Yonit Addissie, Christopher Chun Yu Mak   +2 more
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DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

American Journal of Medical Genetics, Part A, 2003
Katrin Õunap
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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome

American Journal of Medical Genetics, Part A, 2017
Marta Unolt, Elaine Zackai, Scott Adzick   +2 more
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Molecular genetics of 22q11.2 deletion syndrome

American Journal of Medical Genetics, Part A, 2018
Peter Scambler, Joris Vermeesch, Bernice Morrow   +2 more
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22q11.2 Deletion Syndrome: Are Motor Deficits More Than Expected for IQ Level?

Journal of Pediatrics, 2010
Kevin Antshel, Wendy Kates, Robert J Shprintzen   +2 more
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Communication issues in 22q11.2 deletion syndrome: Children at risk

Genetics in Medicine, 2001
Elaine Zackai, Cynthia Solot, Donna Mcdonald-Mcginn Ms Lcgc   +2 more
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Autosomal dominant “Opitz” GBBB syndrome due to a 22q11. 2 deletion

American Journal of Medical Genetics Part A, 1995
David Lynch, Kathleen Sullivan
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