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Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita

Bone marrow transplantation (Basingstoke), 2011-01, Vol.46 (1), p.98-104

2011

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Oral and dental phenotype of dyskeratosis congenita

Oral diseases, 2008-07, Vol.14 (5), p.419-427

2008

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Fanconi's anemia and malignancies

American journal of hematology, 1996-10, Vol.53 (2), p.99-110

Alter, Blanche P.

1996

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VACTERL-H Association and Fanconi Anemia

Molecular syndromology, 2013-02, Vol.4 (1-2), p.87-93

2013

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FANCONI'S ANAEMIA AND ITS VARIABILITY

British journal of haematology, 1993-09, Vol.85 (1), p.9-14

Alter, B. P.

1993

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Embryonic Hemoglobins Are Expressed in Definitive Cells

Blood, 1999-07, Vol.94 (1), p.359-361

1999

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Bone marrow transplant in Diamond-Blackfan anemia

Bone marrow transplantation (Basingstoke), 1998-05, Vol.21 (9), p.965-965

Alter, B P

1998

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Molecular medicine and bone marrow failure syndromes

The Journal of pediatrics, 2000-03, Vol.136 (3), p.275-276

Alter, Blanche P.

2000

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Telomere length is associated with disease severity and declines with age in dyskeratosis congenita

Haematologica (Roma), 2012-03, Vol.97 (3), p.353-359

2012

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TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita

American journal of human genetics, 2008-02, Vol.82 (2), p.501-509

2008

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Pregnancy in bone marrow failure syndromes: Diamond‐Blackfan anaemia and Shwachman‐Diamond syndrome

British journal of haematology, 1999-10, Vol.107 (1), p.49-54

1999

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Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the α globin cluster

Human molecular genetics, 2001-02, Vol.10 (4), p.371-382

2001

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Dyskeratosis Congenita

Dermatologic clinics, 1995-01, Vol.13 (1), p.33-39

1995

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Modern review of congenital hypoplastic anemia

Journal of pediatric hematology/oncology, 2001-08, Vol.23 (6), p.383-384

Alter, B P

2001

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Telomere length in inherited bone marrow failure syndromes

Haematologica (Roma), 2015-01, Vol.100 (1), p.49-54

2015

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Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2

Journal of Medical Genetics, 2007-01, Vol.44 (1), p.1-9

2007

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Treatment of dyskeratosis congenita with Granulocyte Colony‐Stimulating Factor and Erythropoietin

British journal of haematology, 1997-05, Vol.97 (2), p.309-311

1997

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Cancer risks in Fanconi anemia : findings from the German Fanconi Anemia Registry

Haematologica (Roma), 2008-04, Vol.93 (4), p.511-517

2008

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Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to patients with Fanconi anemia : A pilot study

Blood, 1996-09, Vol.88 (5), p.1588-1593

1996

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Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?

British journal of haematology, 1993-11, Vol.85 (3), p.627-630

1993

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Dyskeratosis congenita: Nails and hands

American journal of hematology, 1998-08, Vol.58 (4), p.298-298

1998

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Arm anomalies and bone marrow failure may go hand in hand

The Journal of hand surgery (American ed.), 1992-05, Vol.17 (3), p.566-571

Alter, Blanche P.

1992

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Bone Marrow Failure Syndromes

Clinics in laboratory medicine, 1999-03, Vol.19 (1), p.113-134

Alter, Blanche P.

1999

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Biology of Erythropoiesis

Annals of the New York Academy of Sciences, 1994-01, Vol.731 (1), p.36-47

ALTER, BLANCHE P.

1994

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Arms and the man or hands and the child: congenital anomalies and hematologic syndromes

Journal of pediatric hematology/oncology, 1997-07, Vol.19 (4), p.287-291

Alter, B P

1997

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Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita

Oral and dental phenotype of dyskeratosis congenita

Fanconi's anemia and malignancies

VACTERL-H Association and Fanconi Anemia

FANCONI'S ANAEMIA AND ITS VARIABILITY

Embryonic Hemoglobins Are Expressed in Definitive Cells

Bone marrow transplant in Diamond-Blackfan anemia

Molecular medicine and bone marrow failure syndromes

Telomere length is associated with disease severity and declines with age in dyskeratosis congenita

TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita

Pregnancy in bone marrow failure syndromes: Diamond‐Blackfan anaemia and Shwachman‐Diamond syndrome

Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the α globin cluster

Dyskeratosis Congenita

Modern review of congenital hypoplastic anemia

Telomere length in inherited bone marrow failure syndromes

Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2

Treatment of dyskeratosis congenita with Granulocyte Colony‐Stimulating Factor and Erythropoietin

Cancer risks in Fanconi anemia : findings from the German Fanconi Anemia Registry

Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to patients with Fanconi anemia : A pilot study

Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?

Dyskeratosis congenita: Nails and hands

Arm anomalies and bone marrow failure may go hand in hand

Bone Marrow Failure Syndromes

Biology of Erythropoiesis

Arms and the man or hands and the child: congenital anomalies and hematologic syndromes

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