Yapılan tıbbi araştırmalar insan DNA'sinde yer alan 16. KROMOZOMDAKİ kırılgan bölgenin "Kısırlık" sebebi olduğunu ortaya koymaktadır.
"Summary
The significance of the fragile site on 16 (q21q22) has not yet been fully evaluated. New data will contribute to the understanding of this cytogenetic finding. Therefore we report on four families where a chromosome 16 with fragile site was segregating and such problems as infertility, abortions, malformations, and ancuploidy were present. "
"Summary
The significance of the fragile site on 16 (q21q22) has not yet been fully evaluated. New data will contribute to the understanding of this cytogenetic finding. Therefore we report on four families where a chromosome 16 with fragile site was segregating and such problems as infertility, abortions, malformations, and ancuploidy were present. "
Cystic Fibrosis, 7. KROMOZOMDA yer alan CFTR geninin mutasyonu sonucunda oluşan ve infertiliteye ( Kısırlık ) sebebiyet veren bir hastalıktır.
""Cystic Fibrosis" is one of the most well known genetic mutation disorders. It occurs when there is a mutation in the CFTR gene (located on the 7th chromosome). "
"Abstract - "Cystic Fibrosis" as a cause of INFERTILITY
Cystic fibrosis (CF) is one of the autosomal recessive diseases, caused by mutations in a gene known as cystic fibrosis transmembrane regulator (CFTR). The majority of adult males with CF (99%) is characterized by congenital bilateral absence of vas deferens (CBAVD). CBAVD is encountered in 1-2% of infertile males without CF. Females with CF are found to be less fertile than normal healthy women. In females with CF, delayed puberty and amenorrhoea are common due to malnutrition. CFTR mutations are also associated with congenital absence of the uterus and vagina (CAUV). The National Institutes of Health recommend genetic counseling for any couple seeking assisted reproductive techniques with a CF male or obstructive azoospermia which is positive for a CF mutation."
Cystic fibrosis (CF) is one of the autosomal recessive diseases, caused by mutations in a gene known as cystic fibrosis transmembrane regulator (CFTR). The majority of adult males with CF (99%) is characterized by congenital bilateral absence of vas deferens (CBAVD). CBAVD is encountered in 1-2% of infertile males without CF. Females with CF are found to be less fertile than normal healthy women. In females with CF, delayed puberty and amenorrhoea are common due to malnutrition. CFTR mutations are also associated with congenital absence of the uterus and vagina (CAUV). The National Institutes of Health recommend genetic counseling for any couple seeking assisted reproductive techniques with a CF male or obstructive azoospermia which is positive for a CF mutation."
- Kur'an'da "Akir" / "Akim" ( Kısır ) kelimesi toplam 7 kere tekrarlanmaktadır.
- Kur'an'da ilk "Akir" kelimesi Al'i İmran suresinin 3/40 kodlu ayetinde geçmektedir. ( 3/40 ... 3+4 = "7" )
Al'i İmran 3/40 - Kale (1) rabb (2) i (3) enna (4) yekunü (5) li (6) ı (7) ğulamün (8) ve (9) kad (10)beleğan (11) iye (12) el (13) kiberu (14) ve (15) imraet (16) ı (17) AKIR (18) kale (19) ke (20) zalike (21) allahü (22) yef'alü (23) ma (24) yeşa (25) ( Rab'bim, "Bana yaşlılık ermişken ve karım da kısırken bana nasıl oğlan olur?" dedi. "Allah işte böyle dilediğini yapar." dedi. )
- Ayet kodunu ( 3/40 ) ve ayetteki Akir ( Kısır ) kelimesinin sıra numarasını ( 18 ) oluşturan rakamların toplamının nümerolojik değer 16 olmaktadır.
3+4+0+1+8 = "16"
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