| Familial Hemochromatosis |
Gy31512 |
مشاهده
|
| Fragile. X Syndrome |
Gy31514 |
مشاهده
|
| Fraser Syndrome |
31515 |
مشاهده
|
| Holt-Oram Syndrome (HOS) |
Gy31520 |
مشاهده
|
| Marfan syndrome |
Gy31526 |
مشاهده
|
| Neurofibromatosis type I |
Gy31528 |
مشاهده
|
| Neurofibromatosis type II |
Gy31529 |
مشاهده
|
| Rett Syndrome |
31532 |
مشاهده
|
| Thrombophilia markers |
Gy31533 |
مشاهده
|
| Chromosome Analysis, High Resolution |
3154 |
مشاهده
|
| Amniotic fluid karyotype |
3152 |
مشاهده
|
| Premature ovarian failure |
31530 |
مشاهده
|
| Ambiguous Genitalia Panel |
3151 |
مشاهده
|
| Bardet-Biedl Syndrome (BBS) Panel |
Gy3153 |
مشاهده
|
| Ciliopathy Panel |
Gy3155 |
مشاهده
|
| Comprehensive Inherited Kidney Diseases Panel |
Gy3157 |
مشاهده
|
| Heterotaxy, Situs Inversus and Kartagener's Syndrome Panel |
Gy31519 |
مشاهده
|
| Nephronophthisis and Senior-Loken Syndrome Panel |
31527 |
مشاهده
|
| Combined Pituitary Hormone Deficiency (CPHD) Panel |
3156 |
مشاهده
|
| Congenital Adrenal Hyperplasia (CAH) Panel |
Gy3158 |
مشاهده
|
| Differences of Sex Development (DSD) and Infertility Panel |
3159 |
مشاهده
|
| Differences of Sex Development (DSD) Panel |
31510 |
مشاهده
|
| Female Infertility Panel |
31525 |
مشاهده
|
| Fraser Syndrome Panel |
31516 |
مشاهده
|
| Galactosemia Panel |
Gy31428 |
مشاهده
|
| Hypogonadotropic Hypogonadism.Kallmann Syndrome |
31522 |
مشاهده
|
| Hypospadias |
31523 |
مشاهده
|
| Joubert and Meckel-Gruber Syndromes Panel |
Gy31524 |
مشاهده
|
| Male Infertility Panel |
31525 |
مشاهده
|
| Galactosemia Type I (Classic and Variant Galactosemia) via the GALT Gene |
31518 |
مشاهده
|
| Premature Ovarian Failure (POF) Panel |
31531 |
مشاهده
|
| Primary Ciliary Dyskinesia.Immotile Cilia Syndrome and Cystic Fibrosis Panel |
Gy31469 |
مشاهده
|