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Urinary Prostaglandins and the Effect of Indomethacin on Phosphate Excretion in Children With Hypophosphatemic Rickets

Pediatric research, 2008-08, Vol.64 (2), p.210-212

2008

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Infrequency of MDM2 gene amplification in pediatric solid tumors and lack of association with p53 mutations in adult squamous cell carcinomas

Cancer research (Chicago, Ill.), 1993-12, Vol.53 (24), p.6028-6030

1993

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Linkage of β -thalassaemia mutations and β -globin gene polymorphisms with DNA polymorphisms in human β -globin gene cluster

Nature (London), 1982-04, Vol.296 (5858), p.627-631

1982

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Hemophilia A. Detection of molecular defects and of carriers by DNA analysis

The New England journal of medicine, 1985-10, Vol.313 (14), p.842-848

1985

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Infrequency ofras,p53, WT1, or RB gene alterations in Wilms tumors

Cancer, 1993-12, Vol.72 (12), p.3732-3738

1993

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Quantification of the close association between DNA haplotypes and specific β -thalassaemia mutations in Mediterraneans

Nature (London), 1984-07, Vol.310 (5973), p.152-154

1984

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Allelic loss at chromosomes 3p, 8p, 13q, and 17p associated with poor prognosis in head and neck cancer

JNCI : Journal of the National Cancer Institute, 1994-10, Vol.86 (20), p.1524-1529

1994

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Huntington's Disease: Two Families with Differing Clinical Features Show Linkage to the G8 Probe

Science (American Association for the Advancement of Science), 1985-08, Vol.229 (4715), p.776-779

1985

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Allelic Loss at Chromosomes 3p, 8p, 13q, and l7p Associated With Poor Prognosis in Head and Neck Cancer

JNCI : Journal of the National Cancer Institute, 1994-10, Vol.86 (20), p.1524-1529

1994

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Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the Von-Hippel Lindau tumor suppressor gene in head and neck cancer

Oncogene, 1996-01, Vol.12 (2), p.365-369

1996

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Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors

Cancer, 1993-12, Vol.72 (12), p.3732-3738

1993

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p53, retinoblastoma, and human papillomavirus in squamous cell carcinoma and adjacent normal mucosa of the upper aerodigestive tract

Archives of otolaryngology--head & neck surgery, 1993-10, Vol.119 (10), p.1125-1131

1993

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The Spectrum of β-Thalassemia Genes in China and Southeast Asia

Blood, 1986-10, Vol.68 (4), p.964-966

1986

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p53 mutations, O6‐alkylguanine DNA alkyltransferase activity, and sensitivity to procarbazine in human brain tumors

Cancer, 1995-03, Vol.75 (6), p.1339-1342

1995

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Evidence for Multiple Origins of the βE-globin Gene in Southeast Asia

Proceedings of the National Academy of Sciences - PNAS, 1982-11, Vol.79 (21), p.6608-6611

1982

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Nonrandom Distribution of N-myc Oncogene Genotypes in Neuroblastoma

JNCI : Journal of the National Cancer Institute, 1991-08, Vol.83 (15), p.1085-1088

1991

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β -globin Locus is Linked to the Parathyroid Hormone (PTH) Locus and Lies between the Insulin and PTH Loci in Man

Proceedings of the National Academy of Sciences - PNAS, 1983-11, Vol.80 (21), p.6615-6619

1983

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Use of Oligonucleotide Hybridization in the Characterization of a β°-Thalassemia Gene (β37 TGG→TGA) in a Saudi Arabian Family

Blood, 1986-04, Vol.67 (4), p.1185-1188

1986

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Concordance of a Point Mutation 5’ to the Aγ-Globin Gene With Aγß+Hereditary Persistence of Fetal Hemoglobin in Greeks

Blood, 1986-02, Vol.67 (2), p.551-554

1986

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The Entire β-Globin Gene Cluster Is Deleted in a Form of γδβ-Thalassemia

Blood, 1983-06, Vol.61 (6), p.1269-1274

1983

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Concordance of a Point Mutation 5′ to the Gγ Globin Gene With Gγβ+ Hereditary Persistence of Fetal Hemoglobin in the Black Population

Blood, 1984-12, Vol.64 (6), p.1292-1296

1984

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Recurrence of focal segmental glomerulosclerosis in renal allograft: An in-depth review

Pediatric transplantation, 2010-05, Vol.14 (3), p.314-325

2010

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Impact of Alendronate on Quality of Life in Children With Osteogenesis Imperfecta

Journal of pediatric orthopaedics, 2005-11, Vol.25 (6), p.786-791

2005

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The effect of rhGH on height velocity and BMI in children with CKD: a report of the NAPRTCS registry

Pediatric nephrology (Berlin, West), 2009-09, Vol.24 (9), p.1711-1717

2009

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Bisphosphonate use in children with bone disease

Journal of the American Academy of Orthopaedic Surgeons, 2006-11, Vol.14 (12), p.638-644

2006

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Urinary Prostaglandins and the Effect of Indomethacin on Phosphate Excretion in Children With Hypophosphatemic Rickets

Infrequency of MDM2 gene amplification in pediatric solid tumors and lack of association with p53 mutations in adult squamous cell carcinomas

Linkage of β -thalassaemia mutations and β -globin gene polymorphisms with DNA polymorphisms in human β -globin gene cluster

Hemophilia A. Detection of molecular defects and of carriers by DNA analysis

Infrequency ofras,p53, WT1, or RB gene alterations in Wilms tumors

Quantification of the close association between DNA haplotypes and specific β -thalassaemia mutations in Mediterraneans

Allelic loss at chromosomes 3p, 8p, 13q, and 17p associated with poor prognosis in head and neck cancer

Huntington's Disease: Two Families with Differing Clinical Features Show Linkage to the G8 Probe

Allelic Loss at Chromosomes 3p, 8p, 13q, and l7p Associated With Poor Prognosis in Head and Neck Cancer

Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the Von-Hippel Lindau tumor suppressor gene in head and neck cancer

Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors

p53, retinoblastoma, and human papillomavirus in squamous cell carcinoma and adjacent normal mucosa of the upper aerodigestive tract

The Spectrum of β-Thalassemia Genes in China and Southeast Asia

p53 mutations, O6‐alkylguanine DNA alkyltransferase activity, and sensitivity to procarbazine in human brain tumors

Evidence for Multiple Origins of the βE-globin Gene in Southeast Asia

Nonrandom Distribution of N-myc Oncogene Genotypes in Neuroblastoma

β -globin Locus is Linked to the Parathyroid Hormone (PTH) Locus and Lies between the Insulin and PTH Loci in Man

Use of Oligonucleotide Hybridization in the Characterization of a β°-Thalassemia Gene (β37 TGG→TGA) in a Saudi Arabian Family

Concordance of a Point Mutation 5’ to the Aγ-Globin Gene With Aγß+Hereditary Persistence of Fetal Hemoglobin in Greeks

The Entire β-Globin Gene Cluster Is Deleted in a Form of γδβ-Thalassemia

Concordance of a Point Mutation 5′ to the Gγ Globin Gene With Gγβ+ Hereditary Persistence of Fetal Hemoglobin in the Black Population

Recurrence of focal segmental glomerulosclerosis in renal allograft: An in-depth review

Impact of Alendronate on Quality of Life in Children With Osteogenesis Imperfecta

The effect of rhGH on height velocity and BMI in children with CKD: a report of the NAPRTCS registry

Bisphosphonate use in children with bone disease

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