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American Journal of Medical Genetics
|
February 15, 1993
Aase syndrome: novel radiographic features
A V Hing, S B Dowton
American Journal of Human Genetics
|
August 1, 1993
VNTR and microsatellite polymorphisms within the subtelomeric region of 7q
A V Hing, C Helms, H Donis-Keller
Clinical Genetics
|
February 1, 1992
A lethal syndrome resembling branchio-oculo-facial syndrome
A V Hing, R Torack, S B Dowton
American Journal of Diseases of Children (1960)
|
July 1, 1989
Pulse oximetry in methemoglobinemia
M F Watcha, M T Connor, A V Hing
Journal of Medical Genetics
|
May 1, 1997
Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects
S B Dowton, A V Hing, V Sheen-Kaniecki, et al.
American Journal of Medical Genetics
|
August 28, 1995
Linkage of preaxial polydactyly type 2 to 7q36
A V Hing, C Helms, R Slaugh, et al.
American Journal of Medical Genetics
|
March 30, 1999
GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease
T Pehlivan, B R Pober, M Brueckner, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 18, 2013
Clinical care in craniofacial microsomia: a review of current management recommendations and opportunities to advance research
C L Heike, A V Hing, C A Aspinall, et al.
Nature Genetics
|
November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E Belloni, M Muenke, E Roessler, et al.
Genomics
|
September 15, 1996
Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions
A Vocero-Akbani, C Helms, J C Wang, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics
|
February 15, 1993
Aase syndrome: novel radiographic features
A V Hing, S B Dowton
American Journal of Human Genetics
|
August 1, 1993
VNTR and microsatellite polymorphisms within the subtelomeric region of 7q
A V Hing, C Helms, H Donis-Keller
Clinical Genetics
|
February 1, 1992
A lethal syndrome resembling branchio-oculo-facial syndrome
A V Hing, R Torack, S B Dowton
American Journal of Diseases of Children (1960)
|
July 1, 1989
Pulse oximetry in methemoglobinemia
M F Watcha, M T Connor, A V Hing
Journal of Medical Genetics
|
May 1, 1997
Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects
S B Dowton, A V Hing, V Sheen-Kaniecki, et al.
American Journal of Medical Genetics
|
August 28, 1995
Linkage of preaxial polydactyly type 2 to 7q36
A V Hing, C Helms, R Slaugh, et al.
American Journal of Medical Genetics
|
March 30, 1999
GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease
T Pehlivan, B R Pober, M Brueckner, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 18, 2013
Clinical care in craniofacial microsomia: a review of current management recommendations and opportunities to advance research
C L Heike, A V Hing, C A Aspinall, et al.
Nature Genetics
|
November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E Belloni, M Muenke, E Roessler, et al.
Genomics
|
September 15, 1996
Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions
A Vocero-Akbani, C Helms, J C Wang, et al.
Page
of 1