Hematology and Oncology

Hb f-Auckland [α2^gγ2⁷ (a4)asp→asn] observed in a caucasian newborn from alabama

Chen, S. S., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 5, p. 531-533 3 p.

Research output: Contribution to journal › Article

Abnormal Hemoglobins

Fetal Hemoglobin

Amino Acids

4 Citations (Scopus)

Hb f-Brooklyn or α₂^gγ2⁶⁶(e10)LYSGLN

Plaseska, D., Li, H. J., Wilson, J. B., Kutlar, F., Kutlar, A., Huisman, T. H. J. & Kulpa, J., Jan 1 1990, In : Hemoglobin. 14, 2, p. 213-216 4 p.

Research output: Contribution to journal › Article

Hemoglobins

Blood

Abnormal Hemoglobins

Electrophoresis

Screening

4 Citations (Scopus)

Hb f-catala or α₂ ^gy2l5(a12)trp →arg

Plaseska, D., Wilson, J. B., Kutlar, F., Font, L., Baiget, H. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 5, p. 511-516 6 p.

Research output: Contribution to journal › Article

compound A 12

Spain

Substitution reactions

Amino Acids

Liquids

11 Citations (Scopus)

Hb f-charlotte, an ^aγ variant with a threonine residue in position γ75 and a glycine residue in position γ136

Plaseska, D., Kutlar, F., Wilson, J. B., Fei, Y. J. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 6, p. 617-625 9 p.

Research output: Contribution to journal › Article

Threonine

Glycine

Blood

Substitution reactions

Genes

6 Citations (Scopus)

Hb f-cle or α₂gγ₂65(e9)lys → asn

Kutlar, A., Kutlar, F., Wilson, J. B., Webber, B. B., Gonzalez Redondo, J. M. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 185-188 4 p.

Research output: Contribution to journal › Article

Abnormal Hemoglobins

Fetal Hemoglobin

Peptide Mapping

Asparagine

Hispanic Americans

7 Citations (Scopus)

HB f-cobb OR α₂^aγ2³7(c3)TRP→GLY

Chen, S. S., Webber, B. B., Kutlar, A., Wilson, J. B. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 6, p. 617-619 3 p.

Research output: Contribution to journal › Article

Hemoglobins

Substitution reactions

Cells

hemoglobin A(0)

10 Citations (Scopus)

HB f-h-Osaka or (_α2g_γ;263(e7)HIS→TYR in a caucasian male infant

Glader, B. E., Zwerdling, D., Kutlar, F., Kutlar, A., Wilson, J. B. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 7-8, p. 769-773 5 p.

Research output: Contribution to journal › Article

Hemoglobin M

Abnormal Hemoglobins

Fetal Hemoglobin

Cyanosis

Newborn Infant

4 Citations (Scopus)

Hb f-jiangsu, the first γ chain variant with a valine -methionine substitution: Αgamma;₂134(h12) val→met

Plaseska, D., Kutlar, F., Wilson, J. B., Webber, B. B., Zeng, Y. T. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 2, p. 177-183 7 p.

Research output: Contribution to journal › Article

methionylmethionine

Valine

Fetal Blood

Methionine

Substitution reactions

HB f-Kingston or α₂ ⁶γ₂55(d6)met→arg in a spanish newborn

Pablos, J. M. D., Wilson, J. B., Kutlar, A., Kutlar, F., Webber, B. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 5, p. 513-516 4 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Fetal Hemoglobin

Amino Acids

10 Citations (Scopus)

Hb f-oakd or α₂gγi₂26(b8)glu → lys

Kleman, K., Lubin, B., Wilson, J. B., Kutlar, A., Webber, B. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 181-183 3 p.

Research output: Contribution to journal › Article

Abnormal Hemoglobins

Fetal Hemoglobin

DEAE-Cellulose Chromatography

Peptide Mapping

Glutamine

4 Citations (Scopus)

Hb f-onoda or α2^gγ2¹⁴⁶(^HC3)histyr a newly discovered fetal hemoglobin variant in a japanese newborn

Harano, T., Harano, K., Doi, K., Ueda, S., Imai, K., Ohba, Y., Kutlar, F. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 2, p. 217-222 6 p.

Research output: Contribution to journal › Article

Fetal Hemoglobin

Gene Order

Globins

High performance liquid chromatography

Reverse-Phase Chromatography

4 Citations (Scopus)

Hb fort worth or α₂27 (b8)glu→glyβ2 in a black family from Canada

Carstairs, K. C., Raulfs, A., Kutlar, A., Chen, S. S., Webber, B. B., Wilson, J. B. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 2, p. 201-205 5 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Chromatography

Amino Acids

Hot Temperature

Hb fulton-georgia [α20(B1)His→Pro; HBA1: C.62A>C]: A new α-Globin variant coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC disease

Zhuang, L., Patel, N., Bryant, S., Kutlar, A., Kutlar, F. & Young, A. N., Sep 12 2013, In : Hemoglobin. 37, 5, p. 481-485 5 p.

Research output: Contribution to journal › Article

Hemoglobin SC Disease

Thalassemia

Globins

Hemoglobins

Genes

8 Citations (Scopus)

HB f-xin-su or ^aγ^t73(e17)asp→his: A new slow-moving fetal hemoglobin variant

Ma, M., Hu, H., Kutlar, F., Wilson, J. B. & Huismn, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 5, p. 473-479 7 p.

Research output: Contribution to journal › Article

Fetal Hemoglobin

Fetal Blood

Ethnic Groups

Blood

Substitution reactions

5 Citations (Scopus)

Hb gainesville-ga or α₂β₂46(cd5) gly→arg; second report

Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 6, p. 623-624 2 p.

Research output: Contribution to journal › Article

Blood Protein Electrophoresis

Abnormal Hemoglobins

Hemoglobin A

Fetal Hemoglobin

High Pressure Liquid Chromatography

1 Citation (Scopus)

Hb g-copenhagen or α₂β ₂47(cd6)asp→asn observed in a black newborn

Chen, S. S., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 4, p. 405-408 4 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Peptide Fragments

Asparagine

Aspartic Acid

Hb g-Taipei or β22(b4)glu → gly in a chinese family livinn the Netherlands

Landman, H., Wilson, J. B., Kutlar, A., Gonzalez Redondo, J. M. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 169-171 3 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Glutamine

Glycine

Amino Acids

9 Citations (Scopus)

Hb Hammersmith [β 42(CD1) Phe→Ser]: Occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies

McMorrow Tuohy, A. M., McKie, V. C., Sabio, H., Kutlar, F., Kutlar, A. & Wilson, J. B., Jan 1 1998, In : Journal of Pediatric Hematology/Oncology. 20, 6, p. 563-566 4 p.

Research output: Contribution to journal › Article

Monozygotic Twins

Mutation

African Americans

Hemolytic Anemia

Oximetry

13 Citations (Scopus)

Hb Hekinan observed in three chinese from macau; identification of the gag→gat mutation in the αl-globin gene

Zhao, W., Wilson, J. B., Webber, B. B., Kutlar, A., Tamagnini, G. P., Kuan, B. & Huisnan, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 6, p. 627-635 9 p.

Research output: Contribution to journal › Article

Macau

Globins

High performance liquid chromatography

Aspartic Acid

Purification

10 Citations (Scopus)

Hb Himeji or α₂^β₂140(h18)ala→asp in a portuguese family

Martins, M. C., Rosado, L., Wilson, J. B., Kutlar, A., Hu, H. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 4, p. 411-415 5 p.

Research output: Contribution to journal › Article

3 Citations (Scopus)

Hb inkster [α85(F6)asp→val] found in a caucasian male with polycythemia

Aguinaga, M. D. P., Kutlar, F., Turner, E. A. & Park, D., Jan 1 2000, In : Hemoglobin. 24, 4, p. 333-339 7 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Globins

hemoglobin Inkster

12 Citations (Scopus)

Hb J-Antakya or α₂β₂65(E9)Lys → Met in a Turkish family and Hb Complutense or α₂β₂127(H5)Gln → Glu in a Spanish family; correction of a previously published identification

Huisman, T. H. J., Wilson, J. B., Kutlar, A., Yang, K. G., Chen, S. S., Webber, B. B., Altay, C. & Martinez, A. V., Jun 5 1986, In : Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular. 871, 2, p. 229-231 3 p.

Research output: Contribution to journal › Article

Substitution reactions

Communication

hemoglobin Complutense

hemoglobin J Antakya

6 Citations (Scopus)

HB j-Lome or α₂β₂59(e3)LYS→ASN in a vietnamese family

Prior, J. F., Raven, J. L., Wilson, J. B., Kutlar, A., Kutlar, F. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 1, p. 79-81 3 p.

Research output: Contribution to journal › Article

Hemoglobin J

Abnormal Hemoglobins

DEAE-Cellulose Chromatography

Vietnam

5 Citations (Scopus)

Hb J- Meerut [α 120 (H3) Ala →Glu (α1)] in a Turkish male

Dinçol, G., Güvenç, S., Elam, D., Kutlar, A. & Kutlar, F., Feb 2 2006, In : International Journal of Medical Sciences. 3, 1, p. 26-27 2 p.

Research output: Contribution to journal › Article

Erythrocyte Count

Globins

Oxygen

Population

hemoglobin J Meerut

5 Citations (Scopus)

HB J-pontoise or α263(E12)ALA→ASPβ2 in four members of a Spanish family

Gonzalez Redondo, J. M., Wilson, J. B., Kutlar, A., Huisman, T. H., Sicilia, A., Romero, C. & Fernandes Fuertes, I., Aug 21 1987, In : Hemoglobin. 11, 1, p. 47-50 4 p.

Research output: Contribution to journal › Article

Hemoglobin J

Hemoglobins

Substitution reactions

Observation

11 Citations (Scopus)

Hb las palms or α₂β₂49(cd8)ser→phe, a mildly unstable hemiglobin variant

Malcorra-Azpiazu, J. J., Balda-Aguirre, H. I., Diaz-Chico, J. C., Hu, H., Wilson, J. B., Webber, B. B., Kutlar, F., Kutlar, A. & Huisman, T. H. J., Jan 1 1988, In : Hemoglobin. 12, 2, p. 163-170 8 p.

Research output: Contribution to journal › Article

High performance liquid chromatography

Electrophoresis

Spain

Hemoglobins

Substitution reactions

7 Citations (Scopus)

Hb lepore-Baltimore in a north sardinian family

Nasala, B., Manca, L., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 3, p. 241-246 6 p.

Research output: Contribution to journal › Article

Abnormal Hemoglobins

Italy

Amino Acids

hemoglobin Lepore Baltimore

9 Citations (Scopus)

Hb M Dothan [β 25/26 (B7/B8)/(GGT/GAG→GAG//Gly/Glu→Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics

Kutlar, F., Hilliard, L. M., Zhuang, L., Patel, N., Eroglu, B., Meiler, S. E., Carmichael, H., Russell, R. B. & Kutlar, A., Nov 1 2009, In : Blood Cells, Molecules, and Diseases. 43, 3, p. 235-238 4 p.

Research output: Contribution to journal › Article

Methemoglobin

Globins

Hemoglobin M

Phenotype

Polymerase Chain Reaction

31 Citations (Scopus)

HB monroe or α₂β₂30(b12)ARG→THR, a variant associated with βthalassemia due to a g→c substitution adjacent to the donor splice site of the first intron

Gonzalez-Redondo, J. M., Stoming, T. A., Kutlar, F., Kutlar, A., Hu, H., Wilson, J. B. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 1, p. 67-74 8 p.

Research output: Contribution to journal › Article

DNA Mutational Analysis

Abnormal Hemoglobins

RNA Splice Sites

Thalassemia

Gene Rearrangement

13 Citations (Scopus)

Hb Natal or α2(minus Tyr-Arg)β2: A high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr → terminating codon) mutation in codon α140

Jogessar, V. B., Westermeyer, K., Webber, B. B., Wilson, J. B., Hu, H., Gonzalez-Redondo, J. M., Kutlar, A. & Huisman, T. H. J., Nov 10 1988, In : BBA - Gene Structure and Expression. 951, 1, p. 36-41 6 p.

Research output: Contribution to journal › Article

kyotorphin

Heme

Codon

Tyrosine

Oxygen

15 Citations (Scopus)

Hb oloc or α₂β₂86(f2)ala → asp, a new high oxygen affinity variant

Indrak, K., Wiedermann, B. F., Batek, F., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 151-155 5 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Aspartic Acid

Alanine

Oxygen

7 Citations (Scopus)

HB p-nilotic or α2(βdelta;2 in a turkish family

Altay, C., Kutlar, A., Wilson, J. B., Webber, B. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 4, p. 395-399 5 p.

Research output: Contribution to journal › Article

Sickle Hemoglobin

Siblings

Hemoglobins

Students

Hemoglobinopathies

14 Citations (Scopus)

Hb Q‐Thailand‐Hb H disease in a chinese living in Geneva, Switzerland: Characterization of the variant and identification of the two α‐thalassemic chromosomes

Beris, P., Huber, P., Miescher, P. A., Wilson, J. B., Kutlar, A., Chen, S. S. & Huisman, T. H. J., Jan 1 1987, In : American Journal of Hematology. 24, 4, p. 395-400 6 p.

Research output: Contribution to journal › Article

Globins

Switzerland

Chromosomes

Chromosome Mapping

Liquid Chromatography

23 Citations (Scopus)

Hb S(c)-β⁺ -thalassaemia: Different mutations are associated with different levels of normal Hb A

Gonzalez-Redondo, J. M., Kutlar, F., Kutlar, A., Stoming, T. A., De Pablos, J. M., Kilinc, Y. & Huisman, T. H. J., Jan 1 1988, In : British Journal of Haematology. 70, 1, p. 85-89 5 p.

Research output: Contribution to journal › Article

Thalassemia

Mutation

Globins

Oligonucleotide Probes

Hematology

11 Citations (Scopus)

Hb saint louis or α₂β₂28(b10)leu→gln in a czechoslovakian Male

Wiedermann, B. F., Indrak, K., Wilson, J. B., Webber, B. B., Yang, K. G., Kutlar, F., Kutlar, A. & Huisman, T. H. J., Jan 1 1986, In : Hemoglobin. 10, 6, p. 673-676 4 p.

Research output: Contribution to journal › Article

Hemoglobin M

Abnormal Hemoglobins

Czechoslovakia

Hematologic Tests

High Pressure Liquid Chromatography

6 Citations (Scopus)

Hb Setif [α94(G1)Asp→Tyr (α2)] Detected in a Turkish Family

Dinçol, G., Elam, D., Kutlar, A. & Kutlar, F., Dec 1 2003, In : Hemoglobin. 27, 4, p. 249-252 4 p.

Research output: Contribution to journal › Article

DNA Mutational Analysis

Abnormal Hemoglobins

Protein Denaturation

Family Health

Turkey

6 Citations (Scopus)

HB shelby [α₂β₂131(h9)GLN→LYS]-βdeg;thalassemia [codon 15 (TGG→TGA)] identified by DNA sequencing

Cürük, M. A., Kutlar, A. & Huisman, T. H. J., Jan 1 1992, In : Hemoglobin. 16, 5, p. 417-419 3 p.

Research output: Contribution to journal › Article

Abnormal Hemoglobins

DNA

26 Citations (Scopus)

Hb sun prae or α₂13o(h13)ala → proβ₂ a new unstable variant occurring in low quantities

Harkness, M., Harkness, D. R., Kutlar, F., Kutlar, A., Wilson, J. B., Webber, B. B., Codrington, J. F. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 5, p. 479-489 11 p.

Research output: Contribution to journal › Article

Solar System

Sun

Globins

Genes

Mutation

6 Citations (Scopus)

Hb zengcg or α2β₂114(g16)leu → met

Plaseska, D., Wilson, J. B., Gu, L. H., Kutlar, F., Huisman, T. H. J., Zeng, Y. T. & Shen, M., Jan 1 1990, In : Hemoglobin. 14, 5, p. 555-557 3 p.

Research output: Contribution to journal › Article

Molecular Sequence Data

Abnormal Hemoglobins

Heterozygote

Amino Acid Sequence

Newborn Infant

32 Citations (Scopus)

Heat shock protein 90 inhibitors prevent lps-induced endothelial barrier dysfunction by disrupting Rhoa signaling

Joshi, A. D., Dimitropoulou, C., Thangjam, G., Snead, C., Feldman, S., Barabutis, N., Fulton, D., Hou, Y., Kumar, S., Patel, V., Gorshkov, B., Verin, A. D., Black, S. M. & Catravas, J. D., Jan 1 2014, In : American journal of respiratory cell and molecular biology. 50, 1, p. 170-179 10 p.

Research output: Contribution to journal › Article

HSP90 Heat-Shock Proteins

tanespimycin

Endothelial cells

Myosin Light Chains

Phosphorylation

10 Citations (Scopus)

Helicobacter pylori Infection in Sickle Cell Disease

Woods, K. F., Onuoha, A., Schade, R. R. & Kutlar, A., Jul 1 2000, In : Journal of the National Medical Association. 92, 7, p. 361-365 5 p.

Research output: Contribution to journal › Article

Sickle Cell Anemia

Helicobacter Infections

Helicobacter pylori

Peptic Ulcer

Abdominal Pain

37 Citations (Scopus)

Hematological observations on arabian SS patients with a homozygosity or heterozygosity for a β^s chromosome with haplotype 31

Kutlar, A., Hattori, Y., Bakioglu, I., Kutlar, F., Huisman, T. H. J. & Kamel, K., Jan 1 1985, In : Hemoglobin. 9, 6, p. 545-557 13 p.

Research output: Contribution to journal › Article

Chromosomes

Haplotypes

Sickle Cell Anemia

Heterozygote

Hemoglobins

45 Citations (Scopus)

Hemoglobin_Bibba or α₂^136Pro β₂, an unstable α chain abnormal hemoglobin

Kleihauer, E. F., Reynolds, C. A., Dozy, A. M., Wilson, J. B., Moores, R. R., Berenson, M. P., Wright, C. S. & Huisman, T. H. J., Jan 22 1968, In : BBA - Protein Structure. 154, 1, p. 220-222 3 p.

Research output: Contribution to journal › Article

Autoanalysis

Congenital Hemolytic Anemia

Abnormal Hemoglobins

Ion Exchange Chromatography

Splenectomy

17 Citations (Scopus)

Hemoglobin binding to Aβ and HBG2 SNP association suggest a role in Alzheimer's disease

Perry, R. T., Gearhart, D. A., Wiener, H. W., Harrell, L. E., Barton, J. C., Kutlar, A., Kutlar, F., Ozcan, O., Go, R. C. P. & Hill, W. D., Feb 1 2008, In : Neurobiology of Aging. 29, 2, p. 185-193 9 p.

Research output: Contribution to journal › Article

gamma-Globins

Fetal Hemoglobin

Poisons

Heme

Single Nucleotide Polymorphism

9 Citations (Scopus)

Hemoglobin Birmingham and hemoglobin Galicia: Two unstable β chain variants characterized by small deletions and insertions

Wilson, J. B., Webber, B. B., Hu, H., Kutlar, A., Kutlar, F., Codrington, J. F., Prchal, J. T., Hall, K. M., De Pablos, J. M., Rodriguez, I. & Huisman, T. H. J., Jan 1 1990, In : Blood. 75, 9, p. 1883-1887 5 p.

Research output: Contribution to journal › Article

DNA-Directed DNA Polymerase

Glutamine

Codon

Leucine

Hemoglobins

2 Citations (Scopus)

Hemoglobin daneshgah-Tehran or α₂72(ef1)his→argβ₂ in an argentinean family

De Weinstein, B. I., Kutlar, A., Webber, B. B., Wilson, J. B. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 4, p. 409-411 3 p.

Research output: Contribution to journal › Article

High pressure liquid chromatography

Abnormal Hemoglobins

Macromolecular Substances

Peptide Fragments

Argentina

2 Citations (Scopus)

Hemoglobin F only syndrome at birth: A case of maternal HbA₂' complicating the diagnosis of β-thalassemia

Yee, M. E. M., Quarmyne, M. O., Segbefia, C., Young, A. N., Zhuang, L. & Kutlar, F., Jan 1 2016, In : Journal of Pediatric Hematology/Oncology. 38, 1, p. e32-e34

Research output: Contribution to journal › Article

Fetal Hemoglobin

Thalassemia

Globins

Mothers

Parturition

2 Citations (Scopus)

Hemoglobin h disease in two turkish females and one iranian newborn

Aksoy, M., Kutlar, A., Kutlar, F., Harano, T., Chen, S. S. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 4, p. 373-384 12 p.

Research output: Contribution to journal › Article

Globins

Hemoglobins

Genes

Chromosomes

Thalassemia

4 Citations (Scopus)

Hemoglobin o-padova or _α230(b11)GLU→LYS_β2 observed in members of a turkish family

Kilinç, Y., Kumi, M., Gurgey, A., Altay, C., Webber, B. B., Wilson, J. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 6, p. 621-625 5 p.

Research output: Contribution to journal › Article

Hemoglobins

Hemoglobin C

Fathers

Siblings

Blood

41 Citations (Scopus)

Hemoglobinopathies among the gond tribal groups of central India; interaction of α and βthalassemia with β chain variants

Gupta, R. B., Tiwary, R. S., Pande, P. L., Kutlar, F., Öner, C., Öner, R. & Huisman, T. H. J., Jan 1 1991, In : Hemoglobin. 15, 5, p. 441-458 18 p.

Research output: Contribution to journal › Article

DNA Mutational Analysis

Molecular Sequence Data

Abnormal Hemoglobins

Hemoglobinopathies

Thalassemia