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Results:
1-7
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Results: 7
Authors:
LaDine, BJ
Simmons, JA
Shrimpton, AE
Hoo, JJ
Citation: Bj. Ladine et al., Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: Exclusion of the aarskog (FGD1) gene as a candidate gene, AM J MED G, 99(3), 2001, pp. 248-251
Authors:
Bacha, F
Hoo, JJ
Citation: F. Bacha et Jj. Hoo, New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay, AM J MED G, 101(1), 2001, pp. 70-73
Authors:
Hoo, JJ
Citation: Jj. Hoo, Medicine and the human genome: The new genetics: Molecular concepts, applications and ramifications, J AM MED A, 286(18), 2001, pp. 2332-2333
Authors:
Shrimpton, AE
Braddock, BR
Hoo, JJ
Citation: Ae. Shrimpton et al., Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31, AM J MED G, 92(2), 2000, pp. 155-156
Authors:
Hoo, JJ
Citation: Jj. Hoo, Anodontia of permanent teeth (OMIM # 206780) and pegged/missing maxillary lateral incisors (OMIM # 150400) in the same family, AM J MED G, 90(4), 2000, pp. 326-327
Authors:
Shrimpton, AE
Daly, KM
Hoo, JJ
Citation: Ae. Shrimpton et al., Mapping of a gene (MRXS9) for X-linked mental Retardation, microcephaly, and variably short stature to Xq12-q21.31, AM J MED G, 84(3), 1999, pp. 293-299
Authors:
Hoo, JJ
Citation: Jj. Hoo, Genetics: A popular guide to the principles of human heredity, J AM MED A, 281(1), 1999, pp. 90-91
Risultati:
1-7
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