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Dodderi S. Krishna Murthy
Observed names:
D S Krishna Murthy,
D. S. Krishna Murthy,
D.S.Krishna Murthy
Observed institutions:
Gujarat University,
ICMR National Institute for Research on Women's Health,
Jahra Hospital,
Ahmedabad Civil Hospital,
Indian Council of Medical Research,
Ministry of Health,
B.J. Medical College
show all 7
OpenAlex ID:
A5103684315
Alagille syndrome with de Novo del(20) (p 11.2)
1992
·
Ahmad S. Teebi
, D. S. Krishna Murthy
, et al.
·
American Journal of Medical Genetics
·
24
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
1996
·
M A Redha
, D S Krishna Murthy
, et al.
·
PubMed
·
20
Down syndrome in Kuwait
2005
·
S. A. Al-Awadi
, T. I. Farag
, et al.
·
American Journal of Medical Genetics
·
18
Disease profile of 400 institutionalized mentally retarded patients in Kuwait
1993
·
T. I. Farag
, S. A. Al‐Awadi
, et al.
·
Clinical Genetics
·
18
Recurrent regular trisomy-21 in two Bedouin families. Parental mosaicism versus genetic predisposition.
1995
·
D S Krishna Murthy
, T I Farag
·
PubMed
·
12
Familial Manic–Depressive Illness with Deleted Short Arm of Chromosome 21: Coincidental or Causal?
1989
·
Magda H. El-Badramany
, Talaat I. Farag
, et al.
·
The British Journal of Psychiatry
·
12
Klinefelter's syndrome, mosaic 46,XX/46,XY/47,XXY/48,XXXY/48,XXYY: a case report.
1986
·
S A Al-Awadi
, A S Teebi
, et al.
·
PubMed
·
11
Down syndrome and trisomy 18 in the bedouins
1988
·
T. I. Farag
, S. A. Al‐Awadi
, et al.
·
American Journal of Medical Genetics
·
10
Thyroid function studies in young Down's syndrome.
1981
·
A M Samuel
, D S Krishna Murthy
, et al.
·
PubMed
·
10
Trisomy 18q: 46, XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46, XY,‐13,+der(13)/t(13;18)(q32;q11)
1980
·
D. S. Krishna Murthy
, Z. M. Patel
, et al.
·
Clinical Genetics
·
10
Down Syndrome in Kuwait: Recurrent Familial Trisomy 21 in Siblings
1998
·
S A Al Awadi
, K K Naguib
, et al.
·
Down Syndrome Research and Practice
·
8
PDF
Robertsonian translocation t dic (14p;22p) with regular trisomy 21: a possible interchromosomal effect?
1987
·
T I Farag
, D S Krishna Murthy
, et al.
·
PubMed
·
7
Frequency of trisomy 21, translocation, mosaicism and familial cases fo Down's syndrome in Bombay.
1981
·
D S Krishna Murthy
, Z M Patel
, et al.
·
PubMed
·
7
Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
1989
·
D S Krishna Murthy
, S K Murthy
, et al.
·
PubMed
·
6
Down syndrome in Ahmedabad: Karyotype analysis in 60 cases
1987
·
Sabita K. Murthy
, D. S. Krishna Murthy
, et al.
·
The Indian Journal of Pediatrics
·
5
Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.
1993
·
F M Mohammed
, D S Krishna Murthy
, et al.
·
PubMed
·
4
Clustering of cri du chat syndrome among the Bedouins
1993
·
Talaat I. Farag
, Sadika A. Al‐Awadi
, et al.
·
American Journal of Medical Genetics
·
3
Trisomy 21 q: 46,XX,21s+/47,XX,+21q−(q22→qter) mosaicism (de novo) in a down syndrome child
1984
·
D. S. Krishna Murthy
, Sabita Roy
, et al.
·
The Indian Journal of Pediatrics
·
3
True hermaphrodite: 46, ;XX/46, XY, clinical, cytogenetic and histopathological studies
1982
·
V. C. Shah
, D. S. Krishna Murthy
, et al.
·
The Indian Journal of Pediatrics
·
3
Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardation
1990
·
D. S. Krishna Murthy
, A. S. Teebi
, et al.
·
The Indian Journal of Pediatrics
·
2
Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature.
1990
·
S J Abulhasan
, A S Teebi
, et al.
·
PubMed
·
2
Localization of nucleolus organizing regions on chromosomes of the hanuman langur, Presbytis entellus entellus (Dufresne), & the bonnet monkey, Macaca radiata.
1983
·
D S Krishna Murthy
, S Roy
, et al.
·
PubMed
·
2
Frequency and pattern of association of acrocentric chromosomes in patients of Down syndrome and their mothers.
1981
·
D S Krishna Murthy
, L M Ambani
·
PubMed
·
2
Down’s Syndrome in Kuwait: Recurrent Familial Trisomy 21 in Sibs
1999
·
S.A. Al-Awadi
, K.K. Naguib
, et al.
·
Medical Principles and Practice
·
1
Multiple recurrence of trisomy 21 in two Bedouin families: Parental gonadal mosaicism or {open_quotes}aneuploidy{close_quotes} gene effect?
1994
·
Talaat I. Farag
, D. S. Krishna Murthy
·
The American Journal of Human Genetics
·
1
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Works count:
31
Citation count:
204
H-index:
10
I10-index:
10
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