Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients with Cleft Lip and/or Palate

Épidémiologie des fentes labio-palatines : expérience du Registre de malformations congénitales d’Alsace entre 1995 et 2006

(2013) B. Doray et al.   ARCHIVES DE PEDIATRIE

Classifying Common Oral Clefts: A New Approach After Descriptive Registration

(2013) Antonius J.M. Luijsterburg et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

Genotype-phenotype analysis of 4q deletion syndrome: Proposal of a critical region

(2012) Eugen-Matthias Strehle et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies

(2012) C-N Lee et al.   BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY

A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated?

(2012) Wies Maarse et al.   JOURNAL OF MEDICAL GENETICS

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

(2011) Hutton M Kearney et al.   GENETICS IN MEDICINE

Ten Years Recording Common Oral Clefts with a New Descriptive System

(2010) Antonius J.M. Luijsterburg et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

(2010) Melanie Manning et al.   GENETICS IN MEDICINE

Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization

(2009) Maja Hempel et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

(2009) M. Shinawi et al.   JOURNAL OF MEDICAL GENETICS

Cleft lip and palate

(2009) Peter A Mossey et al.   LANCET

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

(2008) Nicola Brunetti-Pierri et al.   NATURE GENETICS

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

(2008) Heather C. Mefford et al.   NEW ENGLAND JOURNAL OF MEDICINE