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1970 | 1 |
2000 | 1 |
2024 | 0 |
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Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome.
Eur J Hum Genet. 2000 Nov;8(11):869-74. doi: 10.1038/sj.ejhg.5200553.
Eur J Hum Genet. 2000.
PMID: 11093277
A familial syndrome of short stature associated with facial dysplasia and genital anomalies.
Aarskog D.
Aarskog D.
J Pediatr. 1970 Nov;77(5):856-61. doi: 10.1016/s0022-3476(70)80247-5.
J Pediatr. 1970.
PMID: 5504078
No abstract available.
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