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American Journal of Medical Genetics
AU- Abidi, F., and B.D. Hall and R.G. Cadle and G.L. Feldman and H.A. Lubs and L.V. Ouzts and J.F. Arena and R.E. Stevenson and C.E. Schwartz
TI- "X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21."
SO- American Journal of Medical Genetics 85, no. 3 (1999): 223-229.
UM- ped-Lubs, Herbert A. / AU- Armfield, K., and R. Nelson and H.A. Lubs and B. Hane and R.J. Schroer and F. Arena and C.E. Schwartz and R.E. Stevenson
TI- "X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28."
SO- American Journal of Medical Genetics 85, no. 3 (1999): 236-242.
UM- ped-Lubs, Herbert A. / AU- Cabezas, D.A., and J.F. Arena and R.E. Stevenson and C. Schwartz and S. Goldberg and A.R. Morales and H.A. Lubs
TI- "XLMR database."
SO- American Journal of Medical Genetics 85, no. 3 (1999): 202-205.
UM- pth-Morales, Azorides R. / ped-Lubs, Herbert A. / AU- Chudley, A.E., and D.C. Tackels and H.A. Lubs and J.F. Arena and W.P. Stoeber and S. Kovnats and R.E. Stevenson and C.E. Schwartz
TI- "X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between Xq21.33 and Xq23."
SO- American Journal of Medical Genetics 85, no. 3 (1999): 255-262.
UM- ped-Lubs, Herbert A. / AU- Fleming, L.E., and S. Oquendo and J.A. Bean and R. Tamer and S. Finn and A. Wanner
TI- "Pilot detection study of alpha(1) antitrypsin deficiency in a targeted population."
SO- American Journal of Medical Genetics 103, no. 1 (2001): 69-74.
UM- mdd-Wanner, Adam / epi-Fleming, Lora E. / AU- Hamel, B.C.J., and P. Chiurazzi and H.A. Lubs
TI- "Syndromic XLMR genes (MRXS): Update 2000."
SO- American Journal of Medical Genetics 94, no. 5 (2000): 361-363.
UM- ped-Lubs, Herbert A. / AU- Hane, B., and R.E. Stevenson and J.F. Arena and H.A. Lubs and R.J. Simensen and C.E. Schwartz
TI- "Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22."
SO- American Journal of Medical Genetics 85, no. 3 (1999): 271-275.
UM- ped-Lubs, Herbert A. / AU- Hoffman, W.H., and K. Kovacs and S.B. Li and A.S. Kulharya and B.L. Johnson and M.S. Eidson and W.W. Cleveland
TI- "Kenny-Caffey syndrome and microorchidism."
SO- American Journal of Medical Genetics 80, no. 2 (1998): 107-111.
UM- ped-Eidson, Margaret S. / ped-Cleveland, William W. / AU- Lubs, H.A., and F. Abidi and J.A.B. Bier and D. Abuelo and L. Ouzts and K. Voeller and E. Fennell and R.E. Stevenson and C.E. Schwartz and F. Arena
TI- "XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28."
SO- American Journal of Medical Genetics 85, no. 3 (1999): 243-248.
UM- ped-Lubs, Herbert A. / AU- Lubs, H.A., and P. Chiurazzi and J. Arena and C. Schwartz and L. Tranebjaerg and G. Neri
TI- "XLMR genes: Update 1998."
SO- American Journal of Medical Genetics 83, no. 4 (1999): 237-247.
UM- ped-Lubs, Herbert A. / AU- Town, T., and L. Abdullah and F. Crawford and J. Schinka and P.I. Ordorica and E. Francis and P. Hughes and R. Duara and M. Mullan
TI- "Association of a functional mu-opioid receptor allele (+118A) with alcohol dependency."
SO- American Journal of Medical Genetics 88, no. 5 (1999): 458-461.
UM- mdd-Duara, Ranjan / AU- Town, T., and D. Paris and T.A. Parker and A. Kundtz and J. Tan and R. Duara and M. Gold and F. Crawford and M. Mullan
TI- "Alzheimers disease is not associated with the hypertension genetic risk factors PLA(2) or G protein beta 3, either independently or interactively with apolipoprotein E."
SO- American Journal of Medical Genetics 88, no. 5 (1999): 465-468.
UM- mdd-Duara, Ranjan / AU- Wattanasirichaigoon, D., and M.R. Vesely and P. Duggal and J.C. Levine and E.D. Blume and G.S. Wolff and S.B. Edwards and A.H. Beggs
TI- "Sodium channel abnormalities are infrequent in patients with long QT syndrome: Identification of two novel SCN5A mutations."
SO- American Journal of Medical Genetics 86, no. 5 (1999): 470-476.
UM- ped-Wolff, Grace S. /
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