Alpha-fetoprotein and the prenatal detection of neural tube defects.

Por Milunsky, A
Publicado em 1979

An important clinical approach in detecting the fragile X syndrome.

Por Milunsky, A
Publicado em 1985

Threatened survival of academic-based genetic laboratory services.

Por Milunsky, A
Publicado em 1992

L2, a DNA fragment from Xq24-q27, detects an EcoR1 RFLP (HGM9 no. DXS12).

Por Skare, J, Milunsky, J, Milunsky, A
Publicado em 1989

Mapping the X-linked lymphoproliferative syndrome.

Por Skare, J C, Milunsky, A, Byron, K S, Sullivan, J L
Publicado em 1987

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Por Haddad, B R, Lin, A E, Wyandt, H, Milunsky, A
Publicado em 1996

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).

Por Hoth, C F, Milunsky, A, Lipsky, N, Sheffer, R, Clarren, S K, Baldwin, C T
Publicado em 1993

A microassay for argininosuccinase in cultured cells.

Por Jacoby, L B, Littlefield, J W, Milunsky, A, Shih, V E, Wilroy, R S
Publicado em 1972

The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?

Por Neufeld, E F, Liebaers, I, Epstein, C J, Yatziv, S, Milunsky, A, Migeon, B R
Publicado em 1977

Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy.

Por Jones, L A, Skare, J C, Harding, J A, Cohen, A S, Milunsky, A, Skinner, M
Publicado em 1991

Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAs.

Por vanderSpek, J C, Wyandt, H E, Skare, J C, Milunsky, A, Oppenheim, F G, Troxler, R F
Publicado em 1989

Localisation of the Y chromosome stature gene to a 700 kb interval in close proximity to the centromere

Por Kirsch, S, Weiss, B, Kleiman, S, Roberts, K, Pryor, J, Milunsky, A, Ferlin, A, Foresta, C, Matthijs, G, Rappold, G
Publicado em 2002

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Por Van Camp, G, Van Thienen, M N, Handig, I, Van Roy, B, Rao, V S, Milunsky, A, Read, A P, Baldwin, C T, Farrer, L A, Bonduelle, M
Publicado em 1995

The shorter zinc finger protein ZNF230 gene message is transcribed in fertile male testes and may be related to human spermatogenesis.

Por Zhang, S, Qiu, W, Wu, H, Zhang, G, Huang, M, Xiao, C, Yang, J, Kamp, C, Huang, X, Huellen, K, Yue, Y, Pan, A, Lebo, R, Milunsky, A, Vogt, P H
Publicado em 2001