Prenatal diagnosis of Comel-Netherton syndrome with PGD, case report and review article

Journal of Assisted Reproduction and Genetics

Volumn 28, Issue 7, 2011, Pages 615-620

  Bingol, Banu ^a   Tasdemir, Seval ^b   Gunenc, Ziya ^c   Abike, Faruk ^d   Esenkaya, Semra ^b   Tavukcuoglu, Safak ^b   Berkil, Hakan ^e  

^a ISTANBUL BILIM UNIVERSITY   (Turkey)

^b Fertijin IVF Center   (Turkey)

^c MALTEPE UNIVERSITY   (Turkey)

^d ANKARA NUMUNE HOSPITAL   (Turkey)

^e Genetics Genetic Laboratory   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

LEUPRORELIN; RECOMBINANT FOLLITROPIN; TRIPTORELIN;

ADULT; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; BLASTOMERE; CASE REPORT; COMEL NETHERTON SYNDROME; EMBRYO; FEMALE; FETUS DEATH; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; INFERTILITY; INTRACYTOPLASMIC SPERM INJECTION; LABORATORY TEST; OLIGOASTHENOTERATOSPERMIA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; SEMEN ABNORMALITY;

ADULT; BASE SEQUENCE; BLASTOMERES; EMBRYO TRANSFER; FEMALE; FERTILIZATION IN VITRO; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; NETHERTON SYNDROME; OLIGOSPERMIA; POLYCYSTIC OVARY SYNDROME; PREGNANCY; PREIMPLANTATION DIAGNOSIS; PRENATAL DIAGNOSIS; PROTEINASE INHIBITORY PROTEINS, SECRETORY; SPERM INJECTIONS, INTRACYTOPLASMIC;

EID: 80052423115     PISSN: 10580468     EISSN: 15737330     Source Type: Journal    
DOI: 10.1007/s10815-011-9568-y     Document Type: Review

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