scholarly journals Nuclear organisation in totipotent human nuclei and its relationship to chromosomal abnormality

2008 ◽  
Vol 121 (5) ◽  
pp. 655-663 ◽  
Author(s):  
K. A. Finch ◽  
G. Fonseka ◽  
D. Ioannou ◽  
N. Hickson ◽  
Z. Barclay ◽  
...  
Keyword(s):  
Chromosomal Abnormality ◽  
Nuclear Organisation

Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia

2006 ◽  
Vol 30 (8) ◽  
pp. 1043-1047 ◽  
Author(s):  
M. Daskalakis ◽  
N. Mauritzson ◽  
B. Johansson ◽  
K. Bouabdallah ◽  
F. Onida ◽  
...  
Keyword(s):  
Chromosomal Abnormality ◽  
Chronic Myelomonocytic Leukemia ◽  
Myelomonocytic Leukemia

Two myelodysplastic syndrome cases with the inv(ll)(pl5q23) as a sole chromosomal abnormality

1992 ◽  
Vol 81 (4) ◽  
pp. 512-515 ◽  
Author(s):  
Kinuko Mitani ◽  
Yuko Sato ◽  
Yasuhide Hayashi ◽  
Yasusada Miura ◽  
Kiyoshi Miyagawa ◽  
...  
Keyword(s):  
Myelodysplastic Syndrome ◽  
Chromosomal Abnormality

Acquired idiopathic sideroblastic anemia: A new chromosomal abnormality

1983 ◽  
Vol 9 (4) ◽  
pp. 341-345 ◽  
Author(s):  
Philip Schulman ◽  
Nataline Kardon ◽  
Robert Weiner ◽  
Vincent Vinciguerra ◽  
Daniel R. Budman ◽  
...  
Keyword(s):  
Chromosomal Abnormality ◽  
Sideroblastic Anemia

Deletion of chromosome 15 represents a rare but recurrent chromosomal abnormality in myeloid malignancies

2001 ◽  
Vol 37 ◽  
pp. S115
Author(s):  
J. Dierlamm ◽  
L. Michaux ◽  
G. Schilling ◽  
D. Seeger ◽  
P. Leberecht ◽  
...  
Keyword(s):  
Chromosomal Abnormality ◽  
Chromosome 15 ◽  
Myeloid Malignancies

scholarly journals Alobar holoprosencephaly associated with a rare chromosomal abnormality

Medicine ◽  
2018 ◽  
Vol 97 (29) ◽  
pp. e11521 ◽  
Author(s):  
Crîngu Antoniu Ionescu ◽  
Dan Calin ◽  
Dan Navolan ◽  
Alexandra Matei ◽  
Mihai Dimitriu ◽  
...  
Keyword(s):  
Chromosomal Abnormality

scholarly journals Genetic Basis of Male Infertility

2013 ◽  
Vol 4 (1) ◽  
pp. 37-39 ◽  
Author(s):  
Mosammat Rashida Begum ◽  
Mariya Ehsan
Keyword(s):  
Genetic Testing ◽  
Male Infertility ◽  
Medical Treatment ◽  
Intracytoplasmic Sperm Injection ◽  
Chromosomal Abnormality ◽  
Genetic Disease ◽  
Genetic Basis ◽  
Common Cause ◽  
Near Future ◽  
Spermatogenic Failure

Infertility is a couple's problem. Almost 50% case males are responsible for infertility. Most common cause is oligospermia and azoospermia and approximately 5% to 15% of men with azoospermia and severe oligospermia may have a chromosomal abnormality. Men with significant spermatogenic compromise are the candidates of intracytoplasmic sperm injection (ICSI). Raised FSH level above 9 is an indication of spermatogenic compromise. So, medical treatment for these patients is waste of time and money. Early attempt of assisted reproduction is ideal to avoid the crisis of total spermatogenic failure in near future. But before going for ICSI genetic testing if possible and proper counseling about possibilities of transmission of genetic disease to offspring is necessary. DOI: http://dx.doi.org/10.3329/akmmcj.v4i1.13683 AKMMC J 2013: 4(1): 37-39  

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