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Standard cisplatin/infusional 5-fluorouracil (PF) vs docetaxel (T) plus PF (TPF) as neoadjuvant chemotherapy for nonresectable locally advanced squamous cell carcinoma of the head andneck (LA-SCCHN): a phase III trial of the EORTC Head and Neck Cancer Group (EORTC #24971)

Journal of clinical oncology, 2004-07, Vol.22 (14_suppl), p.5508-5508

2004

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Standard cisplatin/infusional 5-fluorouracil (PF) vs docetaxel (T) plus PF (TPF) as neoadjuvant chemotherapy for nonresectable locally advanced squamous cell carcinoma of the head andneck (LA-SCCHN): a phase III trial of the EORTC Head and Neck Cancer Group (EORTC #24971)

Journal of clinical oncology, 2004-07, Vol.22 (14_suppl), p.5508-5508

2004

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A novel MSX1 mutation in hypodontia

American journal of medical genetics. Part A, 2004-08, Vol.128A (4), p.401-403

2004

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The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development

Molecular and Cellular Biology, 2006-08, Vol.26 (15), p.5621-5635

2006

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Rett syndrome in females with CTS hot spot deletions: A disorder profile

American journal of medical genetics. Part A, 2005-01, Vol.132A (2), p.117-120

2005

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DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)

European journal of human genetics : EJHG, 2002-10, Vol.10 (10), p.643-648

2002

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A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency

Human molecular genetics, 2002-03, Vol.11 (5), p.599-604

2002

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Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy

Journal of medical genetics, 2005-05, Vol.42 (5), p.e29-e29

2005

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Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita

American journal of human genetics, 1997-03, Vol.60 (3), p.581-587

1997

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Late‐Onset visceral presentation with cardiomyopathy and without neurological symptoms of adult Sanfilippo A syndrome

American journal of medical genetics. Part A, 2003-05, Vol.118A (4), p.382-387

2003

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Clinical and molecular genetic features of congenital spinal muscular atrophy

Annals of neurology, 1996-11, Vol.40 (5), p.731-738

1996

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Unusual molecular findings in autosomal recessive spinal muscular atrophy

Journal of medical genetics, 1996-06, Vol.33 (6), p.469-474

1996

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Cloning and characterization of the promoter region of the murine alpha-4 integrin subunit

DNA and cell biology, 1994-07, Vol.13 (7), p.743-754

1994

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Preußische Jahrbücher

2021

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Esterase. XXI. Es-9, a possibly new polymorphic esterase in Mus musculus genetically linked to es-2

Biochemical genetics, 1975-06, Vol.13 (5-6), p.369-377

1975

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Methane-hydrogen gas seeps, Zambales Ophiolite, Philippines: Deep or shallow origin?

Chemical geology, 1988-12, Vol.71 (1), p.211-222

1988

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Standard cisplatin/infusional 5-fluorouracil (PF) vs docetaxel (T) plus PF (TPF) as neoadjuvant chemotherapy for nonresectable locally advanced squamous cell carcinoma of the head andneck (LA-SCCHN): a phase III trial of the EORTC Head and Neck Cancer Group (EORTC #24971)

Standard cisplatin/infusional 5-fluorouracil (PF) vs docetaxel (T) plus PF (TPF) as neoadjuvant chemotherapy for nonresectable locally advanced squamous cell carcinoma of the head andneck (LA-SCCHN): a phase III trial of the EORTC Head and Neck Cancer Group (EORTC #24971)

A novel MSX1 mutation in hypodontia

The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development

Rett syndrome in females with CTS hot spot deletions: A disorder profile

DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)

A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency

Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: An updated nomenclature for CDG

Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita

Late‐Onset visceral presentation with cardiomyopathy and without neurological symptoms of adult Sanfilippo A syndrome

Clinical and molecular genetic features of congenital spinal muscular atrophy

Unusual molecular findings in autosomal recessive spinal muscular atrophy

Cloning and characterization of the promoter region of the murine alpha-4 integrin subunit

Preußische Jahrbücher

Esterase. XXI. Es-9, a possibly new polymorphic esterase in Mus musculus genetically linked to es-2

Methane-hydrogen gas seeps, Zambales Ophiolite, Philippines: Deep or shallow origin?

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