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0871 INCREASED RISK OF BEHAVIOR PROBLEMS AND POOR QUALITY OF LIFE IN OVERWEIGHT AND OBESE CHILDREN AND ADOLESCENTS WITH SLEEP DISORDERED BREATHING

Sleep (New York, N.Y.), 2017-04, Vol.40 (suppl_1), p.A323-A324

2017

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0872 BODY POSITION EVALUATED DURING SLEEP BY POLYSOMNOGRAPHY IN INFANTS WITH PIERRE ROBIN SEQUENCE

Sleep (New York, N.Y.), 2017-04, Vol.40 (suppl_1), p.A324-A324

2017

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0873 OBSTRUCTIVE SLEEP APNEA IN CHILDREN WITH BECKWITH-WIEDEMANN SYNDROME

Sleep (New York, N.Y.), 2017-04, Vol.40 (suppl_1), p.A324-A324

2017

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0874 SLEEP DISORDERED BREATHING IN CHILDREN WITH REFRACTORY EPILEPSY TREATED WITH VAGUS NERVE STIMULATOR

Sleep (New York, N.Y.), 2017-04, Vol.40 (suppl_1), p.A324-A325

2017

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09:48 AM: Peds OSA Due to Tongue Obstruction: Which Surgery Is Best?

Otolaryngology-head and neck surgery, 2006-08, Vol.135 (2), p.P183-P183

2006

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A 1-day-old boy with a liver mass

Pediatric annals, 2010-06, Vol.39 (6), p.332-335

Listernick, Robert

2010

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A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 Region

Genomics (San Diego, Calif.), 1997-08, Vol.43 (3), p.366-375

1997

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A 1 Mb-sized microdeletion Xq26.2 encompassing the GPC3 gene in a fetus with Simpson–Golabi–Behmel syndrome

European journal of medical genetics, 2011, Vol.54 (3), p.343-347

2011

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A 10-Day-Old Baby with Ambiguous Genitalia

100 Cases in Clinical Pathology and Laboratory Medicine, 2023, p.57-59

2, 2023

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10 rare tumors that warrant a genetics referral

Familial cancer, 2013-03, Vol.12 (1), p.1-18

2013

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109 - Beckwith-Wiedemann Syndrome

Obstetric Imaging, 2018, p.462-466.e1

Galerneau, France

Second Edition, 2018

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11-month-old Overcomes Liver Cancer, Rare Congenital Condition In Chennai's Hospital

Business world (India), 2023-11

2023

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11p Deletions and breakpoints in squamous cell carcinoma: Association with altered reactivity with the UM-E7 antibody

Genes chromosomes & cancer, 1991-07, Vol.3 (4), p.272-282

1991

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11p15.4 Microdeletion Associates with Hemihypertrophy

Case reports in genetics, 2018, Vol.2018, p.2746347-5

2018

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The 11p15.5 chromosomal region: When did the instability occur?

Medical hypotheses, 2018-12, Vol.121, p.21-25

2018

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11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1274-1280

1992

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11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome

Clinical epigenetics, 2014-03, Vol.6 (1), p.6-6, Article 6

2014

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11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency

Pediatrics International, 2015, Vol.57 (3), p.486-491

2015

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11p15 duplication and 13q34 deletion with Beckwith–Wiedemann syndrome and factor VII deficiency

Pediatrics international, 2015-06, Vol.57 (3), p.486-491

2015

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11p15 Epimutations in Pediatric Embryonic Tumors: Insights from a Methylome Analysis

Cancers, 2023-08, Vol.15 (17), p.4256

2023

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11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver–Russell Syndrome

Human mutation, 2017-01, Vol.38 (1), p.105-111

2017

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11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.3148-3154

2007

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An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C

PloS one, 2011-12, Vol.6 (12), p.e29034

2011

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A 12-year-old girl with pneumonia

Pediatric annals, 2010-04, Vol.39 (4), p.188-191

Listernick, Robert

2010

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American Journal Of Medical Genetics. Part A
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0871 INCREASED RISK OF BEHAVIOR PROBLEMS AND POOR QUALITY OF LIFE IN OVERWEIGHT AND OBESE CHILDREN AND ADOLESCENTS WITH SLEEP DISORDERED BREATHING

0872 BODY POSITION EVALUATED DURING SLEEP BY POLYSOMNOGRAPHY IN INFANTS WITH PIERRE ROBIN SEQUENCE

0873 OBSTRUCTIVE SLEEP APNEA IN CHILDREN WITH BECKWITH-WIEDEMANN SYNDROME

0874 SLEEP DISORDERED BREATHING IN CHILDREN WITH REFRACTORY EPILEPSY TREATED WITH VAGUS NERVE STIMULATOR

09:48 AM: Peds OSA Due to Tongue Obstruction: Which Surgery Is Best?

A 1-day-old boy with a liver mass

A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 Region

A 1 Mb-sized microdeletion Xq26.2 encompassing the GPC3 gene in a fetus with Simpson–Golabi–Behmel syndrome

A 10-Day-Old Baby with Ambiguous Genitalia

10 rare tumors that warrant a genetics referral

109 - Beckwith-Wiedemann Syndrome

11-month-old Overcomes Liver Cancer, Rare Congenital Condition In Chennai's Hospital

11p Deletions and breakpoints in squamous cell carcinoma: Association with altered reactivity with the UM-E7 antibody

11p15.4 Microdeletion Associates with Hemihypertrophy

The 11p15.5 chromosomal region: When did the instability occur?

11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood

11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis

11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome

11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency

11p15 duplication and 13q34 deletion with Beckwith–Wiedemann syndrome and factor VII deficiency

11p15 Epimutations in Pediatric Embryonic Tumors: Insights from a Methylome Analysis

11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver–Russell Syndrome

11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations

An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C

A 12-year-old girl with pneumonia

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