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- Neri Giovanni guestEditor. 53
- Francomano Clair A. guestEditor. 48
- Kruszka Paul guestEditor. 46
- Cavalcanti Denise guestEditor. 38
- Prada Carlos E guestEditor. 38
- Schwartz Ida guestEditor. 38
- Lin Angela guestEditor. 37
- Murali Chaya Nautiyal guestEditor. 37
- Solomon Benjamin D. guestEditor. 34
- Deardorff Matthew A. guestEditor. 31
- 616.04205 663
- Medical genetics -- Periodicals 663
- congenital anomalies of the kidney and urinary tract -- monogenic disease causation -- renal developmental gene 2
- 22q11.2 deletion syndrome -- CHARGE syndrome -- CHD7 -- deafblind, genetic counseling -- Kabuki syndrome -- resources -- sensory deficits 1
- 22q11.2 deletion syndrome -- aortic arch anomalies -- congenital heart disease -- conotruncal defects -- ventricular septal defects 1
- 22q11.2 deletion syndrome -- chromosomal microarray analysis -- cleft lip -- cleft palate -- database 1
- 41, XXY* mouse -- chromosomal imbalance -- germ cell loss -- Klinefelter syndrome -- Sertoli cell 1
- 46, XY DSD -- disorders of sex development -- gonadal dysgenesis -- MAP3K1 1
- 47, XXX syndrome -- 47, XYY syndrome -- epidemiology -- Klinefelter syndrome -- Turner syndrome 1
- 47, XXY -- children with Klinefelter syndrome -- fertility in Klinefelter syndrome -- hypogonadism in Klinefelter syndrome -- Klinefelter syndrome 1