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Familial 16q24.3 Microdeletion Involving ANKRD11 Causes a KBG-Like SyndromeSACHAROW, Stephanie; DELING LI; YAO SHAN FAN et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 3, pp 547-552, issn 1552-4825, 6 p.Article

Case Report Supporting That the Barber―Say and Ablepharon Macrostomia Syndromes Could Represent One DisorderHAENSEL, Jennifer; KOHLSCHMIDT, Nicolai; PITZ, Susanne et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 10, pp 2236-2240, issn 1552-4825, 5 p.Article

Challenges in Clinical Interpretation of Microduplications Detected by Array CGH Analysis : Microduplication syndromesSTANKIEWICZ, Pawel; PURSLEY, Amber N; SAU WAI CHEUNG et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 5, pp 1089-1100, issn 1552-4825, 12 p.Article

The clinical utility of enhanced subtelomeric coverage in array CGHBALLIF, Blake C; SULPIZIO, Scott G; LLOYD, Richard M et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 16, pp 1850-1857, issn 1552-4825, 8 p.Article

The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthLYNCH, Sally Ann; FOULDS, Nicola; COSTIGAN, Colm et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 534-539, issn 1018-4813, 6 p.Article

Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2BALLIF, B. C; THEISEN, A; MCDONALD-MCGINN, D. M et al.Clinical genetics. 2008, Vol 74, Num 5, pp 469-475, issn 0009-9163, 7 p.Article

Pontocerebellar Hypoplasia in Association With De Novo 19p13.11p13.12 MicrodeletionGALLANT, Natalie M; BALDWIN, Erin; SALAMON, Noriko et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 11, pp 2871-2878, issn 1552-4825, 8 p.Article

What can we learn from old microdeletion syndromes using array-CGH screening?MOSCA-BOIDRON, A. L; BOUQUILLON, S; MANOUVRIER-HANU, S et al.Clinical genetics. 2012, Vol 82, Num 1, pp 41-47, issn 0009-9163, 7 p.Article

Epigenetic Profiling of the H19 Differentially Methylated Region and Comprehensive Whole Genome Array-Based Analysis in Silver—Russell SyndromeLIN, Shin-Yu; LEE, Chien-Nan; CHEN, Lang-Yao et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 10, pp 2521-2528, issn 1552-4825, 8 p.Article

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHWEIMIN BI; BREMAN, Amy M; VENABLE, Susan F et al.Prenatal diagnosis. 2008, Vol 28, Num 10, pp 943-949, issn 0197-3851, 7 p.Article

Pure subtelomeric microduplications as a cause of mental retardationRUITER, E. M; KOOLEN, D. A; KLEEFSTRA, T et al.Clinical genetics. 2007, Vol 72, Num 4, pp 362-368, issn 0009-9163, 7 p.Article

Aneuploidy detection in single cells using DNA array-based comparative genomic hybridizationDONG GUI HU; WEBB, Graham; HUSSEY, Nicole et al.Molecular human reproduction. 2004, Vol 10, Num 3-4, pp 283-289, issn 1360-9947, 7 p.Article

Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosisKONIALIS, Christopher; HAGNEFELT, Birgitta; SEVASTIDOU, Sophia et al.Prenatal diagnosis. 2011, Vol 31, Num 6, pp 571-577, issn 0197-3851, 7 p.Article

The use of arrays in preimplantation genetic diagnosis and screeningHARPER, Joyce C; HARTON, Gary.Fertility and sterility. 2010, Vol 94, Num 4, pp 1173-1177, issn 0015-0282, 5 p.Article

Delineation of the Proximal 3q Microdeletion SyndromeSIMOVICH, Marcia J; BLAND, Steven D; PEIFFER, Daniel A et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 13, pp 1729-1735, issn 1552-4825, 7 p.Article

A Novel 2.43 Mb Deletion of 7qll.22-qll.23BLYTH, Moira; BEAL, Sarah; SHUWEN HUANG et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 24, pp 3206-3210, issn 1552-4825, 5 p.Article

Genetic analysis of multifocal superficial urothelial cancers by array-based comparative genomic hybridisationKAWANISHI, H; TAKAHASHI, T; INAZAWA, J et al.British journal of cancer. 2007, Vol 97, Num 2, pp 260-266, issn 0007-0920, 7 p.Article

Identification of Chromosome Abnormalities in Subtelomeric Regions by Microarray Analysis : A Study of 5,380 CasesSHAO, Lina; SHAW, Chad A; PURSLEY, Amber N et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 17, pp 2242-2251, issn 1552-4825, 10 p.Article

A De Novo 2.1-Mb Deletion of 13q12.11 in a Child With Developmental Delay and Minor Dysmorphic FeaturesDERKALOUSTIAN, VazkenM; RUSSELL, Laura; ARADHYA, Swaroop et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 10, pp 2538-2542, issn 1552-4825, 5 p.Article

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From chromosomes to molecular karyotyping : Interstitial 6q deletion : clinical and array CGH characterisation of a new patientLE CAIGNEC, Cédric; SWILLEN, Ann; VAN ASCHE, Elvire et al.European journal of medical genetics. 2005, Vol 48, Num 3, pp 339-345, issn 1769-7212, 7 p.Article

Deletion and Duplication of 11p13-11p14: Reciprocal Aberrations Derived From a Paternal InsertionDOLAN, Michelle; BERRY, Susan A; RUBIN, Karol R et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 11, pp 2775-2783, issn 1552-4825, 9 p.Article

Array CGH using whole genome amplification of fresh-frozen and formalin-fixed, paraffin-embedded tumor DNALITTLE, Suzanne E; VUONONVIRTA, Raisa; REIS-FILHO, Jorge S et al.Genomics (San Diego, Calif.). 2006, Vol 87, Num 2, pp 298-306, issn 0888-7543, 9 p.Article

Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1THIENPONT, Bernard; DIMITRIADOU, Eftychia; THEODOROPOULOS, Katerina et al.European journal of medical genetics. 2009, Vol 52, Num 6, pp 393-397, issn 1769-7212, 5 p.Article