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Clinical Genetics
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May 1, 1992
Effect of chorionic villus sampling on utilization of prenatal diagnosis in women of advanced maternal age
H Brandenburg, C G Gho, M G Jahoda, et al.
Clinical Genetics
|
May 1, 1992
Dominantly inherited microcephaly, short stature and normal intelligence
R C Hennekam, A van Rhijn, F A Hennekam
Clinical Genetics
|
January 1, 1976
Triploidy syndrome. A report on two live-born (69, XXY) and one still-born (69, XXX) infants
A A Saadi, J F Juliar, J Harm, et al.
Clinical Genetics
|
February 1, 1976
The inheritance of hyperlipoproteinaemia with xanthomatosis. A study of 132 kindreds
A Heiberg, K Berg
Clinical Genetics
|
July 1, 1988
Unstable translocation t(14;21) in a man, inherited as a t(13;14) in one of his daughters
J P Siffroi, F Viguie, F Romani
Clinical Genetics
|
June 7, 2021
Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia
Xiaoli Wei, Wensheng Liu, Xingshen Zhu, et al.
Clinical Genetics
|
June 8, 2021
PKD2 gene variants in Chinese patients with autosomal dominant polycystic kidney disease
Dechao Xu, Rongrong Bian, Suxin Tuo, et al.
Clinical Genetics
|
January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance
M C Silengo, M Biagioli, G L Bell, et al.
Clinical Genetics
|
March 1, 1987
Public records and recognition of genetic disease in Scotland
S Collyer, R De Mey
Clinical Genetics
|
March 1, 1987
Technical and biological aspects of pseudomosaicism and mosaicism
P Møller, E Ormerod
Page
of 718
Search research articles
Search
Showing results (431-440 of 7,173) with videos related to
Sort By:
Page
of 718
Clinical Genetics
|
May 1, 1992
Effect of chorionic villus sampling on utilization of prenatal diagnosis in women of advanced maternal age
H Brandenburg, C G Gho, M G Jahoda, et al.
Clinical Genetics
|
May 1, 1992
Dominantly inherited microcephaly, short stature and normal intelligence
R C Hennekam, A van Rhijn, F A Hennekam
Clinical Genetics
|
January 1, 1976
Triploidy syndrome. A report on two live-born (69, XXY) and one still-born (69, XXX) infants
A A Saadi, J F Juliar, J Harm, et al.
Clinical Genetics
|
February 1, 1976
The inheritance of hyperlipoproteinaemia with xanthomatosis. A study of 132 kindreds
A Heiberg, K Berg
Clinical Genetics
|
July 1, 1988
Unstable translocation t(14;21) in a man, inherited as a t(13;14) in one of his daughters
J P Siffroi, F Viguie, F Romani
Clinical Genetics
|
June 7, 2021
Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia
Xiaoli Wei, Wensheng Liu, Xingshen Zhu, et al.
Clinical Genetics
|
June 8, 2021
PKD2 gene variants in Chinese patients with autosomal dominant polycystic kidney disease
Dechao Xu, Rongrong Bian, Suxin Tuo, et al.
Clinical Genetics
|
January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance
M C Silengo, M Biagioli, G L Bell, et al.
Clinical Genetics
|
March 1, 1987
Public records and recognition of genetic disease in Scotland
S Collyer, R De Mey
Clinical Genetics
|
March 1, 1987
Technical and biological aspects of pseudomosaicism and mosaicism
P Møller, E Ormerod
Page
of 718