Hydrops fetalis due to Homozygosity for α-Thalassemia-1, -(α)-20.5 kb: The First Observation in a Turkish Family | Citedby Results | Acta Haematologica | Karger Publishers

Skip to Main Content

Skip Nav Destination

Hydrops fetalis due to Homozygosity for α-Thalassemia-1, -(α)-20.5 kb: The First Observation in a Turkish Family

Acta Haematol (1989) 81 (3): 169–171.

This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.

Homozygosity for the Mediterranean α-thalassemic deletion (hemoglobin Barts hydrops fetalis)

Nasir A. S. Al-Allawi
Maida Y. Shamdeen
Najeeb S. Rasheed

Annals of Saudi Medicine (2010) 30 (2): 153.

Hb H (β4) Disease in Çukurova, Southern Turkey

Mehmet Akif Çürük

Hemoglobin (2007) 31 (2): 265.

Alpha‐thalassaemia prenatal diagnosis by two PCR‐based methods

M. Kleanthous
K. Kyriacou
A. Kyrri
E. Kalogerou
PH. Vassiliades
A. Drousiotou
I. Kallikas
P. Ioannou
M. Angastiniotis

Prenatal Diagnosis (2001) 21 (5): 413.

Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

David H.K. Chui
John S. Waye

Blood (1998) 91 (7): 2213.

Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

David H.K. Chui
John S. Waye

Blood (1998) 91 (7): 2213.

Evaluations of Patients with Recurrent Pregnancy Loss

EDWARD A. TROTT
ELISA M. BENZONI
LEO PLOUFFE

Journal of Women's Health (1996) 5 (6): 567.

-(α)20.5is the Host Frequent Large Deletion in the Puglia Region of Italy

A. Massa
G. Pecci
R. Grubessi
C. Peschle
A. Pietrapertosa
D. Campanale
N. Tannoia

Hemoglobin (1994) 18 (4-5): 353.

5 α-Thalassaemia

Douglas R. Higgs

Baillière's Clinical Haematology (1993) 6 (1): 117.

A PCR‐based strategy to detect the common severe determinants of α thalassaemia

D. K. Bowden
M. A. Vickers
D. R. Higgs

British Journal of Haematology (1992) 81 (1): 104.

The Types of Hemoglobins and Globin Chains in Hydrops Fetalis

F. Kutlar
A. L. Reese
Y. E. Hsia
K. M. Kleman
T. H. J. Huisman

Hemoglobin (1989) 13 (7-8): 671.