| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0022-3476(84)80481-3 |
| P698 | PubMed publication ID | 6726517 |
| P2093 | author name string | R A Pagon | |
| C W Biedel | |||
| J O Zapata | |||
| P2860 | cites work | Female pseudohermaphrodism: a description of 2 unusual cases | Q73205661 |
| Nuclear sex and genital malformation in 48 cases of renal agenesis, with especial reference to nonspecific female pseudoheramphroditism | Q78722466 | ||
| Bilateral absence of the kidneys and ureters. Three cases reported in one family | Q33587617 | ||
| The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia | Q34216747 | ||
| Familial bilateral renal agenesis and hereditary renal adysplasia | Q34217925 | ||
| Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome | Q40570633 | ||
| A community of human malformation syndromes involving the müllerian ducts, distal extremities, urinary tract, and ears | Q54510964 | ||
| A form of intersexuality. | Q55504036 | ||
| Absent Vas Deferens Associated With Renal Agenesis | Q69462462 | ||
| The association of bilateral and unilateral renal aplasia in the same family | Q69702615 | ||
| FamiliaI aggregation in bilateral renal agenesis | Q69766185 | ||
| Klippel-Feil syndrome with renal agenesis and other anomalies | Q70622168 | ||
| Hereditary urogenital adysplasia | Q71433493 | ||
| A familial syndrome of renal, genital, and middle ear anomalies | Q72015291 | ||
| An XXsex chromosome complement in an infant having male-type external genitals, renal agenesis, and other anomalies | Q72822918 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | renal agenesis | Q669435 |
| P304 | page(s) | 861-864 | |
| P577 | publication date | 1984-06-01 | |
| P1433 | published in | The Journal of Pediatrics | Q7743611 |
| P1476 | title | Müllerian anomalies and renal agenesis: autosomal dominant urogenital adysplasia | |
| P478 | volume | 104 |
| Q33678881 | Chromosome 22q11 deletion presenting as the Potter sequence |
| Q44564362 | Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay |
| Q36018505 | Mayer-Rokitansky-Kuster-Hauser syndrome diagnosed by magnetic resonance imaging. Role of imaging to identify and evaluate the uncommon variation in development of the female genital tract |
| Q21203017 | Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome |
| Q84504618 | Our 10-year experience of variable Müllerian anomalies and its management |
| Q41439858 | Relationship between Mayer-Rokitansky-Küster (MRK) anomaly and hereditary renal adysplasia (HRA) |
| Q36710631 | Solid pseudopapillary tumor of the pancreas and concomitant urogenital malformations in a young woman |
| Q25255341 | The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches |
| Q37322404 | The unilateral urogenital anomalies (UUA) rat: a new mutant strain associated with unilateral renal agenesis, cryptorchidism, and malformations of reproductive organs restricted to the left side |
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