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D J Halley

Showing results (31-40 of 96) with videos related to

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Prenatal Diagnosis|November 14, 1997
Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studiesC Van den Berg, S K Ramlakhan, D Van Opstal, et al.
Human Molecular Genetics|December 14, 2001
TSC2 missense mutations inhibit tuberin phosphorylation and prevent formation of the tuberin-hamartin complexM Nellist, B Verhaaf, M A Goedbloed, et al.
The Journal of Clinical Investigation|February 1, 1994
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotypeH J Veeze, D J Halley, J Bijman, et al.
Laboratory Animals|July 1, 1997
The Han:SPRD rat is not a genetic model of human autosomal dominant polycystic kidney disease type 1J Nauta, M A Goedbloed, T M Luider, et al.
Lancet (London, England)|August 16, 1997
Genetic counselling before intracytoplasmic sperm injectionP A In't Veld, D J Halley, J O van Hemel, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Phenotype-karyotype-genotype correlations in Prader-Willi and Angelman syndromes: preliminary resultsA Cecconi, D J Halley, A Salvi, et al.
American Journal of Medical Genetics|March 21, 1998
Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated casesL A Laan, D J Halley, A T den Boer, et al.
Clinical Genetics|September 1, 1979
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repairD J Halley, W Keijzer, N G Jaspers, et al.
The Journal of Biological Chemistry|December 10, 1999
Characterization of the cytosolic tuberin-hamartin complex. Tuberin is a cytosolic chaperone for hamartinM Nellist, M A van Slegtenhorst, M Goedbloed, et al.
Acta Biochimica Polonica|January 1, 1996
Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndromeM Milewski, M Zygulska, J Bal, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|November 14, 1997
Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studiesC Van den Berg, S K Ramlakhan, D Van Opstal, et al.
Human Molecular Genetics|December 14, 2001
TSC2 missense mutations inhibit tuberin phosphorylation and prevent formation of the tuberin-hamartin complexM Nellist, B Verhaaf, M A Goedbloed, et al.
The Journal of Clinical Investigation|February 1, 1994
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotypeH J Veeze, D J Halley, J Bijman, et al.
Laboratory Animals|July 1, 1997
The Han:SPRD rat is not a genetic model of human autosomal dominant polycystic kidney disease type 1J Nauta, M A Goedbloed, T M Luider, et al.
Lancet (London, England)|August 16, 1997
Genetic counselling before intracytoplasmic sperm injectionP A In't Veld, D J Halley, J O van Hemel, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Phenotype-karyotype-genotype correlations in Prader-Willi and Angelman syndromes: preliminary resultsA Cecconi, D J Halley, A Salvi, et al.
American Journal of Medical Genetics|March 21, 1998
Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated casesL A Laan, D J Halley, A T den Boer, et al.
Clinical Genetics|September 1, 1979
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repairD J Halley, W Keijzer, N G Jaspers, et al.
The Journal of Biological Chemistry|December 10, 1999
Characterization of the cytosolic tuberin-hamartin complex. Tuberin is a cytosolic chaperone for hamartinM Nellist, M A van Slegtenhorst, M Goedbloed, et al.
Acta Biochimica Polonica|January 1, 1996
Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndromeM Milewski, M Zygulska, J Bal, et al.
Pageof 10