The chemistry of synthetic dyes and pigments.

Por Lubs, H. A.
Publicado em 1955

A marker X chromosome.

Por Lubs, H A
Publicado em 1969

R banding

Por Verma, R. S., Lubs, H. A.
Publicado em 1975

A simple R banding technic.

Por Verma, R S, Lubs, H A
Publicado em 1975

Quantitative Variations of Haptoglobins in a Caucasian Family

Por Higashi, G. I., Lubs, H. A.
Publicado em 1966

Length heteromorphisms of fluorescent (f) and non-fluorescent (nf) segments of human Y chromosome: classification, frequencies, and incidence in normal Caucasians.

Por Verma, R S, Dosik, H, Scharf, T, Lubs, H A
Publicado em 1978

Localization of spherocytosis to chromosome 8 or 12 and report of a family with spherocytosis and a reciprocal translocation.

Por Kimberling, W J, Fulbeck, T, Dixon, L, Lubs, H A
Publicado em 1975

V/SCAN

Por Golab, T.J., Ledley, R.S., Buas, M., Lubs, H.A.
Publicado em 1988

A new gene (DYX3) for dyslexia is located on chromosome 2

Por Fagerheim, T., Raeymaekers, P., Tonnessen, F. E., Pedersen, M., Tranebjarg, L., Lubs, H.
Publicado em 1999

A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25

Por Cabezas, D., Slaugh, R., Abidi, F., Arena, J, Stevenson, R., Schwartz, C., Lubs, H.
Publicado em 2000

A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58

Por Abidi, F, Holinski-Feder, E, Rittinger, O, Kooy, F, Lubs, H, Stevenson, R, Schwartz, C
Publicado em 2002

Golabi‐Ito‐Hall syndrome results from a missense mutation in the WW domain of the PQBP1 gene

Por Lubs, H, Abidi, F E, Echeverri, R, Holloway, L, Meindl, A, Stevenson, R E, Schwartz, C E
Publicado em 2006

Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.

Por Stevenson, R E, Häne, B, Arena, J F, May, M, Lawrence, L, Lubs, H A, Schwartz, C E
Publicado em 1997

A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.

Por Pai, G S, Hane, B, Joseph, M, Nelson, R, Hammond, L S, Arena, J F, Lubs, H A, Stevenson, R E, Schwartz, C E
Publicado em 1997

Renpenning syndrome maps to Xp11.

Por Stevenson, R E, Arena, J F, Ouzts, E, Gibson, A, Shokeir, M H, Vnencak-Jones, C, Lubs, H A, May, M, Schwartz, C E
Publicado em 1998

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Por Lynch, E D, Ostermeyer, E A, Lee, M K, Arena, J F, Ji, H, Dann, J, Swisshelm, K, Suchard, D, MacLeod, P M, Kvinnsland, S, Gjertsen, B T, Heimdal, K, Lubs, H, Møller, P, King, M C
Publicado em 1997