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1. Ketogenic diets in clinical psychology: examining the evidence and implications for practice.

4. Reducing diagnostic turnaround times of exome sequencing for families requiring timely diagnoses

5. Corrigendum: TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human

6. TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human

7. Severe X-linked chondrodysplasia punctata in nine new female fetuses

8. Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases

11. TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human

12. The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome

13. Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations

14. Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome

15. Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies

16. Spectrum of mutations in the renin–angiotensin system genes in autosomal recessive renal tubular dysgenesis

17. Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations

20. Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios: Role of the Renin-Angiotensin System

22. Prenatal diagnosis of Juberg-Hayward syndrome

23. Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

25. Prenatal presentation of Aicardi‐Goutières syndrome: Nonspecific phenotype necessitates exome sequencing for definitive diagnosis

26. Diagnostic strategy in segmentation defect of the vertebrae: a retrospective study of 73 patients

27. Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

28. Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations

31. Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases

34. Changes in Maternal Blood Inflammatory Markers As a Predictor Of Chorioamnionitis: A Prospective Multicenter Study

35. NovelKIF7mutations extend the phenotypic spectrum of acrocallosal syndrome

36. Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis

39. Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis

40. Unique survival in chrondrodysplasia-hermaphrodism syndrome

41. Prenatal overgrowth and mosaic trisomy 15q25‐qter including the IGF1 receptor gene

50. Torture: The Need for a Dialogue with Its Victims and Its Perpetrators

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